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Soil arthropod biodiversity in plain and hilly olive orchard agroecosystems, in Crete, Greece

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V. D. Gkisakis, D. Kollaros, E. M. Kabourakis
V. D. Gkisakis, D. Kollaros, E. M. Kabourakis


Soil arthropod biodiversity was monitored in 24 olive orchards located in eight different sites in Messara, Crete, covering the two main agroecological zones of olive oil production, hilly and plain. Monitoring was done weekly for five weeks per season, from autumn 2011 to summer 2012, using pitfall traps. Subgroups of functional taxa were defined with respect to services of biological pest control and of nutrient cycling. Comparison of the different agroecological zones in terms of abundance and diversity of soil arthropods and functional subgroups was performed. Coleoptera (39.52%), Formicidae (27.3%), Araneae (8.77%) and Collembola (5.32%) were the most abundant taxa found in the olive orchards. Hilly orchards presented higher total arthropod diversity, but lower abundance due to family Tenebrionidae. Arthropod richness did not differ between agroecological zones. Functional arthropods were a major part of total abundance (76.7%) and presented a trend of higher catches abundance in the hilly orchards arthropods with seasonally statistically significant differences. Shannon Index of Diversity showed higher arthropod diversity in the hilly orchards, being significantly higher in spring. The less intensive olive production in hilly areas appeared to favour soil arthropod diversity.


olive; soil arthropods; diversity; functional biodiversity; olive agroecosystem; agroecological zone

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Allen, W.R. and E.A.C. Hagley. 1990. Epigeal arthropods as predators of mature larvae and pupae of the apple maggot (Diptera, Tephritidae). Environ. Entomol. 19: 309-312.

Altieri, M. 1999. The ecological role of biodiversity in agroecosystems. Agric. Ecos. Environ. 74: 19–31.

Bàrberi, P. 2013. “Functional Agrobiodiversity: The Key to Sustainability?”. In: Agricultural Sustainability-Progress and Prospects in Crop Research. Ed. by Bhullar S.G. and K.N. Bhullar. Elsevier, London, Waltham, San Diego, pp. 3-20.

Bateman, M.A. 1972. The ecology of fruit flies. Ann. Rev. Entomol. 17: 493–518.

Biaggini, M., R. Consorti, L. Dapporto, M. Dellacasa, E. Paggetti and C. Corti. 2007. The taxonomic level order as a possible tool for rapid assessment of Arthropod diversity in agricultural landscapes. Agric. Ecos. Environ. 122: 183–191.

Bigler, F., P. Neuenschwander V. Delucchi and S.E. Michelakis. 1986. Natural enemies of preimaginal stages of Dacus oleae Gmel. (Dipt., Tephritidae) inWestern Crete II: impact on olive fruit fly populations. Boll. Lab. Entomol. Agrar. Filippo Silvestri 43: 79–96.

Brussaard, L., de P. Ruiter and G. Brown. 2007. Soil biodiversity for agricultural sustainability. Agric. Ecos. Environ. 121: 233–244.

Cavalloro, R. and G. Delrio. 1976. Observation on the distribution and survival of Dacus oleae pupae in the soil. Redia 56: 167–76.

Cotes, B., M. Campos, F. Pascual, P.A. García and F. Ruano. 2010. Comparing taxonomic levels of epigeal insects under different farming systems in Andalusian olive agroecosystems. Appl. Soil Ecol. 44: 228-236.

Daane, K.M. and M.W. Johnson. 2010. Olive fruit fly: Managing an ancient pest in modern times. Ann. Rev. Entomol. 55: 151–169.

Fattorini, S. 2008. A multidimensional characterization of rarity applied to the Aegean tenebrionid beetles (Coleoptera Tenebrionidae). J. Insect Conserv. 12: 251–263.

Gonçalves, M.F. and J.A. Pereira. 2012. Abundance and diversity of soil arthropods in the olive grove ecosystem. J. Insect Sci. 12: 1–14.

Hennessey, M.K. 1997. Predation on wandering larvae and pupae of Caribbean fruit fly (Diptera: Tephritidae) in guava and carambola grove soils. J. Agric. Entomol. 14: 129-138.

Hodgson, P.J., J. Sivinski, G. Quintero and M. Aluja. 1998. Depth of pupation and survival of fruit fly (Anastrepha spp.: Tephritidae) pupae in a range of agricultural habitats. Environ. Entomol. 27: 1310-1314.

Kabourakis, E. 1996. “Prototyping and dissemination of ecological olive production systems: A methodology for designing and a first step towards validation and dissemination of prototype ecological olive production systems (EOPS) in Crete”. Published PhD thesis. Wageningen Agricultural University. The Netherlands.

Kabourakis, E. 1999. Code of practices for ecological olive production systems. Olivae 77: 46–55.

McGill, B.J., R.S. Etienne, J.S. Gray, D. Alonso, M.J. Anderson, H.K. Benecha, M. Dornelas, B.J. Enquist, J. Green, F. He, A. Hurlbert, A.E. Magurran, P.A. Marquet, B.A. Maurer, A. Ostling, C.U. Soykan, K. Ugland and E. White. 2007. Species abundance distributions: moving beyond single prediction theories to integration within an ecological framework. Ecol. Letters 10: 995–1015.

Magurran, A.E. 2004. Measuring Biological Diversity. Blackwell, Oxford.

Metzidakis, I., A. Martinez-Vilela, G. Castro Nieto and B. Basso. 2008. Intensive olive orchards on sloping land: Good water and pest management are essential. J. Environ. Manag. 89: 120–128.

Moonen, A., and P. Bàrberi. 2008. Functional Biodiversity: An Agroecosystem Approach. Agric. Ecos. Environ. 127: 7–21.

Moore, J.C., D.E. Walter and H.W. Hunt. 1988. Arthropod regulation of microand mesobiota in below-ground detrital food webs. Ann. Rev. Entomol. 33: 419- 435.

Morris, T., and M. Campos. 1999. Predatory insects in olive-grove soil. Zool. Baetica 10: 149–160.

Morris, T., W. Symondson, N. Kidd and M. Campos. 1999. Las arañas y su incidencia sobre Prays oleae en el olivar. Boll. Sanid. Veg. Plagas 25: 475–489.

Orsini, M.M., K.M. Daane, K.R. Sime and E.H. Nelson. 2007. Mortality of olive fruit fly pupae in California. Bioc. Sci. Technol. 17: 797–807.

Petersen, H. and M. Luxton. 1982. A comparative analysis of soil fauna populations and their role in decomposition processes. Oikos 39: 288-388.

Reichle, D.E. 1977. The role of soil invertebrates in nutrient cycling. Ecol. Bull. 145-156.

Ruano, F., C. Lozano, P. Garcia, A. Peña, A. Tinaut, F. Pascual and M. Campos, 2004. Use of arthropods for the evaluation of the olive orchard management regimes. Agric. Forest Entomol. 6: 111-120.

Santos, S., J. Cabanas and J. Pereira. 2007. Abundance and diversity of soil arthropods in olive grove ecosystem (Portugal): Effect of pitfall trap type. Eur. J. Soil Biol. 43: 77–83.

Stork, N.E. and P. Eggleton. 1992. Invertebrates as determinants and indicators of soil quality. Am. J. Alternative Agric. 7: 38-47.

Thomas, D.B. 1995. Predation on the soilinhabiting stages of the Mexican fruitfly (Diptera, Tephritidae). Southwest. Entomol. 20: 61-71.

Urbaneja, A., F. García Marí, D. Tortosa, C. Navarro, P. Vanaclocha, L. Bargues and P. Castañera. 2006. Influence of ground predators on the survival of the Mediterranean fruit fly pupae, Ceratitis capitata, in Spanish citrus orchards. Biocontrol 51: 611-626.

Vassiliou, A. 2000. Farm structure optimisation of, and the impact of widespread conversion to ecological olive production systems. PhD Thesis, University of Wales.

Volakakis, N. 2010. Development of strategies to improve the quality and productivity of organic and “low input” olive production systems in semi-arid Mediterranean regions. PhD thesis, University of Newcastle Upon Tyne.

Volakakis, N.G., M.D. Eyre and E.M. Kabourakis. 2012. Olive Fly Bactrocera oleae (Diptera, Tephritidae) Activity and fruit infestation under mass trapping in an organic table olive orchard in Crete, Greece. J. Sustain. Agric. 36: 683–698.

Wong, T.T.Y., D.O. McInnis, J.I. Nashimotoa, A.K. Ota and V.C.S. Chang. 1984. Predation of the Mediterranean fruit fly (Diptera: Tephritidae) by the Argentine ant (Hymenoptera: Formicidae) in Hawaii. J. Econ. Entomol. 77: 1454-1458.

Wurst, S. 2013. Plant-mediated links between detritivores and aboveground herbivores. Front Plant Sci. 4: 380.


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