Skip to main content

Comparison of Ant Community Diversity and Functional Group Composition Associated to Land Use Change in a Seasonally Dry Oak Forest

Abstract

Ants have been used to assess land use conversion, because they reflect environmental change, and their response to these changes have been useful in the identification of bioindicators. We evaluated ant diversity and composition associated to different land use change in a temperate forest (above 2000 m asl) in Mexico. The study was carried out in “Flor del Bosque” Park a vegetation mosaic of native Oak Forests and introduced Eucalyptus and grasslands. Species richness, dominance and diversity rarefaction curves, based on ant morphospecies and functional groups, were constructed and compared among the three vegetation types, for the rainy and the dry seasons of 2008–2009. Jaccard and Sorensen incidence-based indices were calculated to obtain similarity values among all the habitats. The Oak Forest was a rich dominant community, both in species and functional groups; the Eucalyptus plantation was diverse with low dominance. The most seasonality habitat was the grassland, with low species and high functional group diversity during the dry seasons, but the reverse pattern during the wet season. The Oak Forest was more similar to the Eucalyptus plantation than to the grassland, particularly during the dry season. Oak Forests are dominated by Cold Climate Specialists, specifically Prenolepis imparis (Say). The Eucalyptus and the grassland are characterized by generalized Myrmicinae, as Pheidole spp. and Monomorium ebenium (Forel). The conservation of the native Oak Forest is primordial for the maintenance of Cold Climate Specialist ant communities. The microclimatic conditions in this forest, probably, prevented the invasion by opportunistic species.

This is a preview of subscription content, access via your institution.

Fig 1
Fig 2

References

  • Agosti D, Alonso LE (2000) The ALL protocol: a standard protocol for the collection of ground-dwelling ants. In: Agosti D, Majer JD, Alonso L, Shultz T (eds) Ants: standard methods for measuring and monitoring biodiversity. Smithsonian Institution Press, Washington DC, pp 204–222

    Google Scholar 

  • Andersen AN (1990) The use of ant communities to evaluate change in Australian terrestrial ecosystems: a review and a recipe. P Ecol Soc Aust 16:347–357

    Google Scholar 

  • Andersen AN (1997) Functional groups and patterns of organization in North American ant communities: a comparison with Australia. J Biogeogr 24:433–460

    Article  Google Scholar 

  • Andersen AN (2000) A global ecology of rain forest ants: functional groups in relation to stress and disturbance. In: Agosti D, Majer JD, Alonso L, Shultz T (eds) Ants: Standard Methods for Measuring and Monitoring Biodiversity. Smithsonian Institution Press, Washington DC, pp 25–34

    Google Scholar 

  • Andersen AN, Hoffmann BD, Muller WJ, Griffiths AD (2002) Using ants as bioindicators in land management: simplifying assessment of ant community responses. J Appl Ecol 39:8–17

    Article  Google Scholar 

  • Badano EI (2010) El microclima del bosque de encinos y su comparación con zonas deforestadas del parque Estatal Flor del Bosque. Reporte técnico Fondo Mixto-CONACYT-Gobierno del Estado de Puebla (Proyecto 108571), p 18

  • Badano EI, García-Guzmán J, Barranco-León M de las N (2010) Encinos del Parque Estatal General Lázaro Cárdenas del Río Flor del Bosque. Reporte técnico Fondo Mixto-CONACYT-Gobierno del Estado de Puebla (Proyecto 108571), p 28

  • Bestelmeyer B, Wiens JA (1996) The effects of land use on the structure of ground-foraging ant communitites in the Argentine Chaco. Ecol Appl 6:1225–1240

    Article  Google Scholar 

  • Brown WL Jr (2000) Diversity of ants. In: Agosti D, Majer JD, Alonso LE, Schultz TR (eds) Ants standard methods for measuring and monitoring biodiversity. Smithsonian Institution Press, Washington, pp 45–79

    Google Scholar 

  • Chao A, Chadzon RL, Colwell RK, Shen T (2005) A new statistical approach for assessing similarity of species composition with incidence and abundance data. Ecol Lett 8:148–159

    Article  Google Scholar 

  • Chapin FS, Mcguire AD, Randerson J, Pielke R, Baldocchi D, Hobbie SE, Roulet N, Eugster W, Kasischke E, Rastetter EB, Zimov SA, Running SW (2000) Arctic and boreal ecosystems of western North America as components of the climate system. Glob Change Biol 6:1–13

    Article  Google Scholar 

  • Coelho MS, Fernandes GW, Santos JC, Delabie JHC (2009) Ants (Hymenoptera: Formicidae) as Bioindicators of Land Restoration in a Brazilian Atlantic Forest Fragment. Sociobiology 54:51–63

    Google Scholar 

  • Colwell RK (2006) EstimateS: statistical estimation of species richness and shared species from samples. Version 8. User’s guide and application. http/purl.oclc.org/estimates. Accessed 9 Dec 2014

  • Costes-Quijano R, Meza AR, Macías-Juárez A, Berriel-Mastreta CA, Cortés-Atílano B, Martínez-Romero LE, Hernández-Bautista R (2006) Plan de manejo parque ecológico recreativo General Lázaro Cárdenas “Flor del Bosque”. Secretaría de Medio Ambiente y Recursos Naturales. Gobierno del Estado de Puebla, Puebla, México, p 105

    Google Scholar 

  • INEGI (Instituto Nacional de Estadística et al. Geografía, México). (2010). Mapa de climas. http://mapserver.inegi.gob.mx/geografia/espanol/estados/pue/clim.cfm?c=444&e=31. Accessed November 19, 2010

  • Del Toro I, Ribbons RR, Pelini SL (2012) The little things that run the world revisited: a review of ant-mediated ecosystem services and disservices (Hymenoptera: Formicidae). Myrmecological News 17:133–146

    Google Scholar 

  • Dolek M, Freese-Hager A, Bussler H, Floren A, Liegl A, Schmidl J (2009) Ants on oaks: effects of forest structure on species composition. J Insect Conserv 13:367–375

    Article  Google Scholar 

  • Ellison AM (2012) The ants of Nantucket: unexpectedly high biodiversity in an anthropogenic landscape. Northeast Nat 19:43–66

    Article  Google Scholar 

  • Fellers JH (1989) Daily and seasonal activity in woodland ants. Oecologia 78:69–76

    Article  Google Scholar 

  • Flores-Maldonado KY, Phillips SA Jr, Sánchez-Ramos G (1999) The myrmecofauna (Hymenoptera: Formicidae) along an altitudinal gradient in the Sierra Madre Oriental of Northeastern Mexico. The Southwest Nat 44:457–461

    Article  Google Scholar 

  • Gotelli NJ, Colwell RK (2001) Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness. Ecol Lett 4:379–391

    Article  Google Scholar 

  • Gotelli, NJ, Entsminger JL (2005) EcoSim: null models software for ecology. Version 7.71. Acquired Intelligence Inc & Kesey-Bear. Jericho, VT 05465. http://homepages.together.net/~gentsmin/ecosim.htm

  • Houdeshell H, Friedrich RL, Philpott SM (2011) Effects of prescribed burning on ant nesting ecology in Oak Savannas. Am Midl Nat 166:98–111

    Article  Google Scholar 

  • Izhaki I, Levey DJ, Silva WR (2003) Effects of prescribed fire on ant community in Florida pine savanna. Ecol Entomol 28:439–448

    Article  Google Scholar 

  • Lynch JF, Balinsky EC, Vail SG (1980) Foraging patterns in three sympatric forest ant species, Prenolepis imparis, Paratrechina melanderi and Aphaenogaster rudis (Hymenoptera: Formicidae). Ecol Entomol 5:353–371

    Article  Google Scholar 

  • Majer JD (1983) Ants: bioindicators of mine site rehabilitation, land use and land conservation. Environ Manage 7:375–383

    Article  Google Scholar 

  • Manos PS, Stanford AM (2001) The historical biogeography of Fagaceae: tracking the tertiary history of temperate and subtropical forests of the northern hemisphere. Int J Plant Sci 162:S77–S93

    Article  Google Scholar 

  • Nixon KC (1993) The genus Quercus in México. In: Ramamoorthy TP, Bye R, Lot A, Fa J (eds) Biological diversity of Mexico: origins and distribution. Oxford University Press, London, pp 447–458

    Google Scholar 

  • Nixon KC (2006) Global and Neotropical Distribution and Diversity of Oak (genus Quercus) and Oak Forests Ecological Studies. In: Kappelle M (ed) Ecology and Conservation of Neotropical Montane Oak Forests. Springer-Verlag, Berlin Heidelberg, 185:4–13

  • Rico-Gray V (1993) Use of plant derived food resources by ants in the dry tropical Lowlands of Coastal Veracruz, Mexico. Biotropica 25:301–315

    Article  Google Scholar 

  • Rzedowski J (2006) Vegetación de México. Limusa, DF, p 505

  • Sala OE, Chapin FS, Armesto JJ, Berlow E, Bloomfield J, Dirzo R, Huber-Sanwald E, Huenneke LF, Jackson RB, Kinzig A, Leemans R, Lodge DM, Mooney HA, Oesterheld M, Poff NL, Sykes MT, Walker BH, Walker M, Wall DH (2000) Global biodiversity scenarios for the year 2100. Science 287:1770–1774

    CAS  Article  PubMed  Google Scholar 

  • Sawada M (1999) Rookcase v. 0.9.5a.: an excel 97/2000 Visual Basic add-in for exploring global and local spatial autocorrelation. Bull Ecol Soc Am 80:231–234

    Article  Google Scholar 

  • Suguituru SS, Silva RR, Souza DR, Munhae CB, Morini MSC (2011) Ant community richness and composition across a gradient from Eucalyptus plantations to secondary Atlantic Forest. Biota Neotrop 1:369–376

    Article  Google Scholar 

  • Teodoro AV, Sousa-Souto L, Klein AM, Tscharntke T (2010) Seasonal Contrasts in the Response of Coffee Ants to Agroforestry Shade-Tree Management. Environ Entomol 39:1744–1750

    CAS  Article  PubMed  Google Scholar 

  • Toledo VM (1988) La diversidad biológica de México. Ciencia y Desarrollo 81:17–30

    Google Scholar 

  • Tschinkel WR (1987) Seasonal life history and nest architecture of a winter-active ant, Prenolepis imparis. Insect Soc 34:143–164

    Article  Google Scholar 

  • Underwood EC, Fisher BL (2006) The role of ants in conservation monitoring: if, when, and how. Biol Conserv 132:166–182

    Article  Google Scholar 

  • Vasconcelos HL (1999) Effects of forest disturbance on the structure of ground-foraging ant communitites in central Amazonia. Biodivers Conserv 8:409–420

    Google Scholar 

  • Wang C, Strazsnac JS, Butler L (2001) Association between ants (Hymenoptera: Formicidae) and habitat characteristics in oak-dominated mixed forests. Community and Ecosystem Ecology 30:842–848

    Google Scholar 

  • Wheeler WM (1930) The ant Prenolepis imparis say. Ann Entomol Soc Am 23:1–26

    Article  Google Scholar 

  • Yoshimura M (2009) Impact of secondary forest management on ant assemblage composition in the temperate region in Japan. J Insect Conserv 13:563–568

    Article  Google Scholar 

  • Zavala-Chávez F (1998) Observaciones sobre la distribución de encinos en México. Polibotánica 8:47–64

    Google Scholar 

Download references

Acknowledgments

Leonor Lastra and the students of the Entomology Course Summer 2009 helped with fieldwork. Cecilia Martínez Pérez helped with the sorting of ants, under the supervision of Jorge Valenzuela and Luis Quiroz. This research was supported by the grant Fondo Mixto Consejo Nacional de Ciencia y Tecnología - Gobierno del Estado de Puebla PUE-2008-1-108571 to Ernesto I. Badano. The Administration of the State Park and Ecological Reserve Lázaro Cárdenas del Río “Flor del Bosque” granted permission to carry out the study and provided logistic support.

Author information

Affiliations

Authors

Corresponding author

Correspondence to M Cuautle.

Additional information

Edited by Fernando B Noll – UNESP

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Cuautle, M., Vergara, C.H. & Badano, E.I. Comparison of Ant Community Diversity and Functional Group Composition Associated to Land Use Change in a Seasonally Dry Oak Forest. Neotrop Entomol 45, 170–179 (2016). https://doi.org/10.1007/s13744-015-0353-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13744-015-0353-y

Keywords

  • Cold climate specialist
  • functional groups
  • generalized Myrmicinae
  • Prenolepis imparis