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Early establishment and survival of the neotropical dry deciduous forest tree Lysiloma microphyllum from mountainous Bajio Queretano, Mexico

Published online by Cambridge University Press:  13 June 2017

José Guadalupe Hernández-Oria ,
Richard I. Yeaton Hawkins ,
Eduardo Castaño Tostado  and
Víctor L. Barradas
José Guadalupe Hernández-Oria
Affiliation:
Departamento de Ecología Funcional, Laboratorio de Interacción Planta Atmósfera, Instituto de Ecología, Universidad Nacional Autónoma de México. AP 70–275, Circuito Exterior, Ciudad Universitaria, 04510México, D.F.
Richard I. Yeaton Hawkins
Affiliation:
Instituto de Investigación de Zonas Desérticas, Universidad Autónoma de San Luis Potosí, Altair No. 200, Fraccionamiento del Llano, 78377, San Luis Potosí, México
Eduardo Castaño Tostado
Affiliation:
Departamento de Investigación y Posgrado en Alimentos, Facultad de Química, Universidad Autónoma de Querétaro, Cerro de las Campanas s/n, 76010, Querétaro, México
Víctor L. Barradas*
Affiliation:
Departamento de Ecología Funcional, Laboratorio de Interacción Planta Atmósfera, Instituto de Ecología, Universidad Nacional Autónoma de México. AP 70–275, Circuito Exterior, Ciudad Universitaria, 04510México, D.F.
*
*Corresponding author. Email: vlbarradas@ecologia.unam.mx
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Abstract:

The tropical dry deciduous forest (TDF) of the semi-arid region of Bajio in Mexico is dominated by successional communities, in which Lysiloma microphyllum is irregularly distributed, however the environmental factors influencing its establishment have been poorly studied. We conducted field experiments to isolate the impact of three factors on the early life-history stages of this tree. Over a 2-y period, we monitored the effects of (1) predation, (2) understorey light and (3) aspect on germination, seed-to-seedling transition (establishment) and seedling survival, and we found that open space negatively affected germination (14.9 ± 1.5% vs 96 ± 1.5% in shade; mean ± SE), while shade increased seedling establishment and survival (36.9 ± 8.2% vs 4.7 ± 3.8% in open sites). Predation decreased survival and was strongest in open conditions (0 vs 62.7 ± 9.4% in shaded exclosures). In contrast, aspect had little influence on germination and survival. The results suggest that shaded microsites positively affect the early life stages of L. microphyllum, a key process in TDF recovery.

Keywords

microhabitatmortalityseed germinationseedling establishmentsurvivalsecondary tropical dry deciduous forest
Type
Research Article
Information
Journal of Tropical Ecology , Volume 33 , Issue 3 , May 2017 , pp. 213 - 227
Copyright
Copyright © Cambridge University Press 2017 

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References

LITERATURE CITED

ÁLVAREZ-AQUINO, C. & WILLIAMS-LINERA, G. 2012. Seedling survival and growth of tree species: site condition and seasonality in tropical dry forest restoration. Botanical Sciences 90:341–351.Google Scholar
ÁLVAREZ-YÉPIZ, J. C., MARTÍNEZ-YRÍZAR, A., BÚRQUEZ, A. & LINDQUIST, C. 2008. Variation in vegetation and soil properties related to land use history of old-growth and secondary tropical forests in northwestern Mexico. Forest Ecology and Management 256:355–366.Google Scholar
ANDRADE, G., CALDERÓN DE RZEDOWSKI, G., CAMARGO-RICALDE, S.L., GRETHER, R., HERNÁNDEZ, H. M., MARTÍNEZ-BERNAL, A., RICO, L., RZEDOWSKI, J. & SOUSA, M. 2007. Familia Leguminosae. Subfamilia Mimosoideae. Flora del Bajío y de regiones adyacentes. Fascículo 150. Instituto de Ecología-Centro Regional del Bajío, Pátzcuaro, Mich., México. 229 pp.Google Scholar
ARRIAGA, L. & LEÓN, J. L. 1989. The Mexican tropical deciduous forest of Baja California Sur: a floristic and structural approach. Vegetatio 84:45–52.Google Scholar
BARRADAS, V. L. 1991. Radiation regime in a tropical dry deciduous forest in western Mexico. Theoretical and Applied Climatology 44:57–64.Google Scholar
BLAIN, D. & KELLMAN, M. 1991. The effect of water supply on tree seed germination and seedling survival in a tropical seasonal forest in Veracruz, Mexico. Journal of Tropical Ecology 7:69–83.Google Scholar
BRENES-ARGUEDAS, T. 2012. Leaf damage and density-dependent effects on six Inga species on a neotropical forest. Revista de Biología Tropical 60:1503–1512.Google Scholar
BULLOCK, S., MOONEY, H. & MEDINA, E. (eds). 1995. Seasonally dry tropical forests. Cambridge University Press, Cambridge. 450 pp.Google Scholar
CÁRDENAS, I. & CAMPO, J. 2007. Foliar nitrogen and phosphorus reabsorption and decomposition in the nitrogen-fixing tree Lysiloma microphyllum in primary and secondary seasonally tropical dry forests in Mexico. Journal of Tropical Ecology 23:107–113.Google Scholar
COMITA, L. S., QUEENBOROUGH, S. A., MURPHY, S. J., ECK, J. L., XU, K., KRISHNADAS, M., BECKMAN, N. & ZHU, Y. 2014. Testing predictions of the Janzen–Connell hypothesis: a meta-analysis of experimental evidence for distance and density-dependent seed and seedling survival. Journal of Ecology 102:845–856.CrossRefGoogle ScholarPubMed
DE SOUZA GOMES, G. & SCARIOT, A. 2014. Direct seeding of dry forest tree species in abandoned pastures: effects of grass canopy and seed burial on germination. Ecological Research 3:473–482.Google Scholar
GARCÍA, E. 1988. Modificaciones al sistema de Köppen para adaptarlo a las condiciones de la República Mexicana. Instituto de Geografía, UNAM, México. 252 pp.Google Scholar
GERHARDT, K. 1996a. Effects of root competition and canopy openness on survival and growth of tree seedlings in a tropical seasonal dry forest. Forest Ecology and Management 82:33–48.Google Scholar
GERHARDT, K. 1996b. Germination and development of sown mahogany (Swietenia macrophylla King) in secondary tropical dry forest habitat in Costa Rica. Journal of Tropical Ecology 12: 275–289.Google Scholar
GERHARDT, K. 1998. Leaf defoliation of tropical dry forest tree seedlings – implications for survival and growth. Trees 13:88–95.Google Scholar
GONZÁLEZ-RIVAS, B., TIGABU, M., CASTRO-MARÍN, G. & ODÉN, P. C. 2009. Seed germination and seedling establishment of Neotropical dry forest species in response to temperature and light conditions. Journal of Forestry Research 20:99–104.Google Scholar
GONZÁLEZ-RUIZ, T., JARAMILLO, V., PEÑA, J. & FLORES, A. 2008. . Nodulation dynamics and nodule activity in leguminous tree species of a Mexican tropical dry forest. Journal of Tropical Ecology 24:107–110.Google Scholar
GOODALE, U. M., BERLYN, G. P., GREGOIRE, T. G., TENNAKOON, K. U. & ASHTON, M. S. 2014. Differences in survival and growth among tropical rain forest pioneer tree seedlings in relation to canopy openness and herbivory. Biotropica 46:183–193.Google Scholar
GRISCOM, H. P. & ASHTON, M. S. 2011. Restoration of dry tropical forests in Central America: a review of pattern and process. Forest Ecology and Management 261:1564–1579.Google Scholar
HAMMOND, D. S. 1995. Postdispersal seed and seedling mortality of tropical dry forest trees after shifting agriculture, Chiapas, Mexico. Journal of Tropical Ecology 11:295–313.Google Scholar
HUANTE, P. & RINCÓN, E. 1998. Responses to light changes in tropical deciduous woody seedlings with contrasting growth rates. Oecologia 113:53–66.Google Scholar
INEGI (Instituto Nacional de Estadística Geografía e Informática). 1986. Noménclator y anexo cartográfico del estado de Querétaro. Secretaría de Programación y Presupuesto. México. 143 pp.Google Scholar
INMAN-NARAHARI, F., OSTERTAG, R., HUBBELL, S., GIARDINA, P., CORDELL, S. & SACK, L. 2016. Density-dependent seedling mortality varies with light availability and species abundance in wet and dry Hawaiian forests. Journal of Ecology 104:773–780.Google Scholar
JIA, X., DAI, X.-F., SHEN, Z.-X., ZHANG, J.-Y. & WANG, G.-X. 2011. Facilitation can maintain clustered spatial pattern of plant populations during density-dependent mortality: insights from a zone-of-influence model. Oikos 120:472–480.Google Scholar
JOHN, R., DATTARAJA, H., SURESH, H. & SUKUMAR, R. 2002. Density-dependence in common tree species in a tropical dry forest in Mudumalai, southern India. Journal of Vegetation Science 13: 45–56.Google Scholar
KHURANA, E. & SINGH, J. S. 2001. Ecology of seed and seedling growth for conservation and restoration of tropical dry forest: a review. Environmental Conservation 28:39–52.Google Scholar
KHURANA, E. & SINGH, J. S. 2004. Germination and seedling growth of five tree species from tropical dry forest in relation to water stress: impact of seed size. Journal of Tropical Ecology 20:385–396.Google Scholar
LABAT, J. N. 1987. Le fourré subtropical et la forêt tropicale caducifoliée du nord-ouest de l´état du Michoacán, Mexique: structure et affinités floristiques. Trace 12:3–11.Google Scholar
LABAT, J. N. 1995. Végétation du Nord-Ouest du Michoacán Mexique. Fascículo Complementario VIII. Instituto de Ecología A.C.-Centro Regional del Bajío. Pátzcuaro, Michoacán, México. 401 pp.Google Scholar
LEE, E. T. 1992. Statistical methods for survival data analysis. Lifetime Leraning Publications, Belmont. 556 pp.Google Scholar
LEÓN DE LA LUZ, J. L., DOMÍNGUEZ-CADENA, R. & MEDEL-NARVÁEZ, A. 2012. Florística de la Selva Baja Caducifolia de la Península de Baja California, México. Botanical Sciences 90:143–162.Google Scholar
LÉVESQUE, M., MCLAREN, K. P. & MCDONALD, M. A. 2011. Recovery and dynamics of a primary tropical dry forest in Jamaica, 10 years after human disturbance. Forest Ecology and Management 262:817–826.Google Scholar
LIEBERMAN, D. & LI, M. 1992. Seedling recruitment patterns in tropical dry forest in Ghana. Journal of Vegetation Science 3:375–382.Google Scholar
LÓPEZ, L. & TERBORGH, J. 2007. Seed predation and seedling herbivory as factors in tree recruitment failure on predator-free forested islands. Journal of Tropical Ecology 23:129–137.Google Scholar
MAROD, D., KUTINTARA, U., TANAKA, H. & NAKASHIZUKA, T. 2004. Effects of drought and fire on seedling survival and growth under contrasting light conditions in a seasonal tropical forest. Journal of Vegetation Science 15:691–700.Google Scholar
McLAREN, K. P. &. McDONALD, M. A. 2003a. Seedling dynamics after different intensities of human disturbance in a tropical dry limestone forest in Jamaica. Journal of Tropical Ecology 19: 567–578.Google Scholar
McLAREN, K. P. & McDONALD, M. A. 2003b. The effects of moisture and shade on seed germination and seedling survival in a tropical dry forest in Jamaica. Forest Ecology and Management 183:61–75.Google Scholar
MIRANDA, F & HERNÁNDEZ-X, E. 1963. Los tipos de vegetación de México y su clasificación. Boletín de la Sociedad Botánica de México 23:29–47.Google Scholar
MIRANDA-JÁCOME, A., MONTAÑA, C. & FORNONI, J. 2013. Sun/shade conditions affect recruitment and local adaptation of a columnar cactus in dry forests Annals of Botany 111:293–303.Google Scholar
MURPHY, P. G. & LUGO, A. E. 1986. Ecology of tropical dry forest. Annual Review of Ecology and Systematics 17:67–88.Google Scholar
POORTER, L. & MARKESTEIJN, L. 2008. Seedling traits determine drought tolerance of tropical tree species. Biotropica 40:321–331.Google Scholar
PYKE, D. A. & THOMPSON, J. N. 1986. Statistical analysis of survival and removal rate experiments. Ecology 67:240–245.Google Scholar
RAY, G. J. & BROWN, B. J. 1995. Restoring Caribbean dry forest: evaluation of tree propagation techniques. Restoration Ecology 3:86–94.Google Scholar
RZEDOWSKI, J. 1978. Vegetación de México. Limusa, México. 432 pp.Google Scholar
RZEDOWSKI, J. & CALDERÓN, G. 1987. El bosque tropical caducifolio de la región mexicana del Bajío. Trace 12:12–21.Google Scholar
RINCÓN, E. & HUANTE, P. 1993. Growth responses of tropical deciduous tree seedlings to contrasting light conditions. Trees Structure and Function 7:202–207.Google Scholar
SÁNCHEZ-VELÁSQUEZ, L. R., QUINTERO-GRADILLAB, S., ARAGÓN-CRUZ, F & PINEDA-LÓPEZ, M. A. R. 2004. Nurses for Brosimum alicastrum reintroduction. Forest Ecology and Management 198:401–404.CrossRefGoogle Scholar
SLOT, M. & POORTER, L. 2007. Diversity of tropical tree seedling responses to drought. Biotropica 39:683–690.Google Scholar
SULLIVAN, J. J. 2003. Density-dependent shoot-borer herbivory increases the age of first reproduction and mortality of neotropical tree saplings. Oecologia 136:96–106.Google Scholar
VARGAS, G., WERDEN, L. & POWERS, J. 2015. Explaining legume success in tropical dry forest based on seed germination niches: a new hypothesis. Biotropica 47:277–280.Google Scholar
VIEIRA, D. & SCARIOT, A. 2006. Principles of natural regeneration of tropical dry forests for restoration. Restoration Ecology 14:11–20.Google Scholar
VIEIRA, D., LIMA, V., SEVILHA, A. & SCARIOT, A. 2008. Consequences of dry-season seed dispersal on seedling establishment of dry forest trees: should we store seeds until the rains? Forest Ecology and Management 256:471–481.Google Scholar
WEBB, C. O. & PEART, D. R. 1999. Seedling density dependence promotes coexistence of Bornean rain forest trees. Ecology 80:2006–2017.Google Scholar
WILLIAMS-LINERA, G., ALVAREZ-AQUINO, C., HERNÁNDEZ-ASCENCIÓN, E. & TOLEDO, M. 2011. Early successional sites and the recovery of vegetation structure and tree species of the tropical dry forest in Veracruz, Mexico. New Forests 42:131–148.Google Scholar
ZAR, J. H. 1999. Biostatistical analysis. Prentice Hall, Upper Saddle River, NJ. 662 pp.Google Scholar
ZIMMERMAN, J. K., WRIGHT, S. J., CALDERÓN, O., APONTE, M. & PATON, S. 2007. Flowering and fruiting phenologies of seasonal and aseasonal neotropical forests: the role of annual changes in irradiance. Journal of Tropical Ecology 23:231–251.Google Scholar