DOI: 10.17151/bccm.2022.26.1.1
How to Cite
Ospina Bautista, F. ., López Bedoya, P. A., Estévez, J. V. ., Martínez Torres, D. ., & Galvis Jiménez, S. . (2022). Restoration strategy drives the leaf litter myriapod richness (Arthropoda: Myriapoda) on a protected area. Boletín Científico. Centro De Museos, 26(1), 13–23. https://doi.org/10.17151/bccm.2022.26.1.1

Authors

Fabiola Ospina Bautista
Universidad de Caldas
Fabiola.Ospina@ucaldas.edu.co
Perfil Google Scholar
Pablo A. López Bedoya
Universidad de Caldas
pablo.lobe19@gmail.com
Perfil Google Scholar
Jaime Vicente Estévez
Universidad de Caldas
Jaime.estevez@ucaldas.edu.co
Perfil Google Scholar
Daniela Martínez Torres
Universidad Nacional de Colombia
sdmartinezt@unal.edu.co
Perfil Google Scholar
Sebastián Galvis Jiménez
Universidad Nacional de Colombia
sgalvisjimenez@gmail.com
Perfil Google Scholar

Abstract

Objective: To determine the leaf litter myriapod community in two restoration strategies of a protective area of Colombia, a secondary forest and an Andean alder plantation. Scope: The knowledge of the biodiversity of invertebrates associated with leaf litter breakdown in restoration forests may contribute to assessing the restoration process efficiency and success. Within this forested soil biodiversity framework, myriapods influence organic matter dynamics by transforming leaf litter (or other plant-derived materials), reducing the surface of decomposition, and affecting decomposer communities and their interactions. Methodology: We designed a leaf litter translocation experiment using leaf litter of Alnus acuminata Kunth and Hedyosmum bonplandianum Kunth, the most abundant species in each restoration strategy underway from the 60s in the Reserva Natural Río Blanco
y Quebrada Olivares, Manizales, Colombia. We measured the myriapod richness and abundance two and four months after beginning the leaf litter decomposition experimental trials. Main results: Classes Diplododa, Chilopoda, and Symphyla colonized the leaf litter in both restoration strategies. The restoration strategy affected myriapod richness, abundance and composition. Myriapod richness and abundance were greater in the Andean alder plantation, millipedes were the most abundance myriapods. Myriapod composition also differs among litter species. The plant composition of each restoration strategy could lead to differences in litterfall quality and, consequently, in the resources available for the colonization of the myriapod community, which contributes directly and indirectly to the decomposition process in the restoration strategies.

Adis, J. (Editor). (2002). Amazonian Arachnida and Myriapoda: Identification keys to all classes, orders, families, some genera, and lists of known terrestrial species. Pensoft Pub.

Aide, T. M., Zimmerman, J. K., Pascarella, J. B., Rivera, L., & Marcano-Vega, H. (2000). Forest regeneration in a chronosequence of tropical abandoned pastures: Implications for restoration ecology. Restoration Ecology, 8(4), 328-338. https://doi.org/10.1046/j.1526-100x.2000.80048.x

Anderson, M. J. (2017). Permutational multivariate analysis of variance(Permanova). In Wiley StatsRef: Statistics Reference Online, pp. 1-15. American Cancer Society. https://doi.org/10.1002/9781118445112.stat07841

Anderson, J.M., S.A. Huish, P. Ineson, M.A. Leonard, & Splatt, P.R. (1985). Interactions of invertebrates, microorganisms and tree roots in nitrogen and mineral element fluxes in deciduous woodland soils, pp. 377-392 In: A.H. Fitter, D. Atkinson, D. J. Read, M.B. Usher (Eds.) Ecological interactions in soil: Plant, Microbes and Animals. Blackwell Publishing.

Barreto da Silva, W., Périco, E., Schmidt Dalzochio, M., Santos, M., & Cajaiba, R. L. (2018). Are litterfall and litter decomposition processes indicators of forest regeneration in the neotropics? Insights from a case study in the Brazilian Amazon. Forest Ecology and Management, 429, 189-197. https://doi.org/10.1016/j.foreco.2018.07.020

Blakely, J. K., D.A. Neher, & Spongberg, A.L. (2002). Soil invertebrate and microbial communities, and decomposition as indicators of polycyclic aromatic hydrocarbon contamination. Applied Soil Ecology, 21(1), 71-88. https://doi.org/10.1016/S0929-1393(02)00023-9

Cajaiba, R. L., Périco, E., Caron, E., Dalzochio, M. S., Silva, W. B., & Santos, M. (2017). Are disturbance gradients in neotropical ecosystems detected using rove beetles? A case study in the Brazilian Amazon. Forest Ecology and Management, 405, 319-327. https://doi.org/10.1016/j.foreco.2017.09.058

Caldeira, M.V.W., R.D. Silva, S.R. Kunz, J.P. Zorzanelli, & Godinho, T.O. (2013). Biomassa e nutrientes da serapilheira em diferentes coberturas florestais. Comunicata Scientiae 4(2),111-119.

Carcamo, H.A., T.A. Abe, C.E. Prescott, F.B. Holl, & Chanway, C.P. (2000). Influence of millipedes on litter decomposition, N mineralization, and microbial communities in a coastal forest in British Columbia, Canada. Canadian Journal of Forest Research, 30(5), 817-826. https://doi.org/10.1139/x00-014

Clarke, K. R. (1993). Non-parametric multivariate analyses of changes in community structure. Austral Ecology, 18(1), 117-143. https://doi.org/10.1111/j.1442-9993.1993.tb00438.x

Cole, R. J., K.D. Holl, R.A. Zahawi, P. Wickey, & Townsend, A.R. (2016). Leaf litter arthropod responses to tropical forest restoration. Ecology and Evolution, 6(15), 5158-5168. https://doi.org/10.1002/ece3.2220

Corpocaldas. (2010). Reserva Forestal Protectora de las Cuencas Hidrógraficas de Río Blanco y Quebrada Olivares. Plan de Manejo.

Coulis, M., S. Hättenschwiler, S. Rapior, & Coq S. (2009). The fate of condensed tannins during litter consumption by soil animals. Soil Biology and Biochemistry, 4, 2573-2578. https://doi.org/10.1016/j.soilbio.2009.09.022

Coulis, M., S. Hättenschwiler, N. Fromin, & David, J.F. (2013). Macroarthropod-micro- organism interactions during the decomposition of Mediterranean shrub litter at different moisture levels. Soil Biology and Biochemistry, 64, 114-121 https://doi.org/10.1016/j.soilbio.2013.04.012

Crawley, M.J. (2007). The R Book: West Sussex. John Wiley & Sons.

Crowther, T.W., L. Boddy, &. Jones, T.H. (2012). Functional and ecological consequences of saprotrophic fungus-grazer interactions. ISME J, 6: 1992-2001. https://doi.org/10.1038/ismej.2012.53

David, J.F., & Gillon, D. (2002). Annual feeding rate of the millipede Glomeris marginata on holm oak (Quercus ilex) leaf litter under Mediterranean conditions. Pedobiologia 46(1),42-52. https://doi.org/10.1078/0031-4056-00112

David, J.F. & Handa, I.T. (2010). The ecology of saprophagous macroarthropods (millipedes, woodlice) in the context of global
change. Biological Reviews, 85(4), 881-895. https://doi.org/10.1111/j.1469-185X.2010.00138.x

David, J. F. (2014). The role of litter-feeding macroarthropods in decomposition processes: A reappraisal of common views. Soil Biology and Biochemistry, 76,109-118. https://doi.org/10.1016/j.soilbio.2014.05.009

FAO (Food and Agriculture Organisation). (2001). State of the World’s Forests 2001.

FAO (Food and Agriculture Organisation). (2015). Evaluación de los recursos forestales mundiales 2015. Second edition.

Filser, J. (2002). The role of Collembola in carbon and nitrogen cycling in soil. Pedobiologia,46(3-4), 234-245. https://doi.org/10.1078/0031-4056-00130

Fox, J. & Weisberg, S. (2011). An {R} Companion to Applied Regression, Second edition. SAGE.

Frasson, J.M.F, J.L.O. Rosado, S.G. Elias, & Harter-Marques, B. (2016). Litter decomposition of two pioneer tree species and associated soil fauna in areas reclaimed after surface coal mining in Southern Brazil. Revista Brasileira de Ciência do Solo, 40(0). https://doi.org/10.1590/18069657rbcs20150444

Fujii, S., & Takeda, H. (2017). Succession of soil microarthropod communities during the aboveground and belowground litter decomposition processes. Soil Biology and Biochemistry, 110, 95-102. https://doi.org/10.1016/j.soilbio.2017.03.003

Gunther, B., B.C. Rall, O. Ferlian, S. Scheu, & Eitzinger, B. (2014). Variations in prey consumption of centipede predators in forest soils as indicated by molecular gut content analysis. Oikos, 123(10), 1192-1198. https://doi.org/10.1111/j.1600-0706.2013.00868.x

Guendehou, G. H., S. Liski, M. Tuomi, M. Moudachirou, B. Sinsin, & Mäkipää, R. (2014). Decomposition and changes in chemical composition of leaf litter of five dominant tree species in a West African tropical forest. Tropical. Ecology,55(2), 207-220. https://core.ac.uk/download/pdf/52269172.pdf

Hall, J., M. S., Ashton, E. J. Garen, E & Jose, S. (2011). The ecology and ecosystem services of native trees: Implications for reforestation and land restoration in Mesoamerica. Forest Ecology and Management, 261(10), 1553-1557. https://doi.org/10.1016/j.foreco.2010.12.011

Hansen, R.A., & Coleman, D.C. (1998). Litter complexity and composition are determinants of the diversity and species composition of oribatid mites (Acari, Oribatida) in litterbags. Applied Soil Ecology, 9(1-3), 17-23. https://doi.org/10.1016/S0929-1393(98)00048-1

Hasegawa, M., & Takeda, H. (1993). Changes in feeding attributes of four collembolan populations during the decomposition process of pine needles. Pedobiologia 39,155-169.

Hobbs, R. J., S. Arico, J. Aronson, J.S. Baron, P. Bridgewater, V.A. Cramer, P.R. Epstein, J.J. Ewel, C.A. Klink, A.E. Lugo, D. Norton, D. Ojima, M.D. Richardson, E. Sanderson, F. Valladares, M. Vilà, R. Zamora, & Zobel, M. (2006). Novel ecosystems: Theoretical and management aspects of the new ecological world order. Global Ecology and Biogeography, 15(1), 1-7. https://doi.org/10.1111/j.1466-822X.2006.00212.x

Irmler, U. (2000). Changes in the fauna and its contribution to mass loss and N release during leaf litter decomposition in two deciduous forests. Pedobiología, 44(2), 105-118. https://doi.org/10.1078/S0031-4056(04)70032-3

Lavelle, P., & Spain, A.V. (2001). Soil Ecology. Kluwer Academic.

Lensing, J. R., & Wise, D.H. (2006). Predicted climate change alters the indirect effect of predators on an ecosystem process. Proceedings of the National Academy of Sciences, 103(42), 15502-15505. https://doi.org/10.1073/pnas.0607064103

Lilleskov, E.A., & Bruns, T.D. (2005). Spore dispersal of a resupinate ectomycorrhizal fungus, Tomentella sublilacina, via soil food webs. Mycologia 97(4), 762-769. http://www.jstor.org/stable/3762225

Mcalpine, C., C.P. Catterall, R. Nally, D. Lindenmayer, J.L. Reid, K.D. Holl, A.F. Bennett, R.K. Runting, K. Wilson, R.J. Hobbs, L. Seabrook, S. Cunningham, A. Moilanen, M. Maron, L. Shoo, I. Lunt, P. Vesk, L. Rumpff, & Martin, T.G. (2016). Integrating plant- and animal- based perspectives for more effective restoration of biodiversity. Frontiers in Ecology and the Environment, 14(1), 37-45. https://doi.org/10.1002/16-0108.1

Oksanen, J., F. G. Blanchet, M. Friendly, R. Kindt, P. Legendre, D. McGlinn, P.R. Minchin, R.B. O’Hara, G.L. Simpson, P. Solymos, M.H. Stevens, E. Szoecs, & Wagner, H. (2018). Vegan: Community Ecology Package. R package vegan, version 2.2-1. https://www.worldagroforestry.org/publication/vegan-community-ecology-package-r-package-vegan-vers-22-1

Paquette, A., & Messier, C. (2010). The role of plantations in managing the world’s forests in the Anthropocene. Frontiers in Ecology and the Environment, 8(1), 27-34. https://doi.org/10.1890/080116

Pramanik, R., K. Sarkar, & Joy, V.C. (2001). Efficiency of detritivore soil arthropods in mobilizing nutrients from leaf litter. Tropical ecology,42(1),51-58.

Patricio, M. S., L.F. Nunes, & Pereira, E.L. (2012). Litterfall and litter decomposition in chestnut high forest stands in northern Portugal. Forest Systems, 21(2), 259. https://doi.org/10.5424/fs/2012212-02711

R Core Team. (2018). R: A language and environment for statistical computing. R Foundation for Statistical Computing. https://www.R-project.org/

Salmon, S., & Geoffroy, J. (2005). Earthworms and Collembola relationships: effects of predatory centipedes and humus forms. Soil Biology and Biochemistry, 37(3), 487-495. https://doi.org/10.1016/j.soilbio.2004.08.011

Santonja, M., A., Aupic-samain, E. Forey, & Chauvat, M. (2018). Increasing temperature and decreasing specific leaf area amplify centipede predation impact on Collembola, European Journal of Soil Biology, 89, 9-13. https://doi.org/10.1016/j.ejsobi.2018.08.002

Scheller, U., & Adis, J. (1996). A pictorial key for the symphylan families and genera of the Neotropical Region south of Central Mexico (Myriapoda, Symphyla). Studies on Neotropical Fauna and Environment, 31(1), 57-61. https://doi.org/10.1076/


Shelley, R. M., & Mercurio, R.A. (2005). Ectonocryptoides quadrimeropus, a new centipede genus and species from Jalisco, Mexico; proposal of Ectonocryptopinae, analysis of subfamilial relationships, and a key to subfamilies and genera of the Scolopocryptopidae (Scolopendromorpha). Zootaxa, 1094(1), 25. https://doi.org/10.11646/zootaxa.1094.1.2

Shiels, A. B., & Walker, L.R. (2003). Bird perches increase forest seeds on Puerto Rican landslides. Restoration Ecology,11(4): 457-465.

Silver, W.L., S.J. Hall, & Gonzáles, G. (2014). Differential effects of canopy trimming and litter deposition on litterfall and nutrient dynamics in a wet subtropical forest. Forest Ecology and Management, 332, 47-55. https://doi.org/10.1016/j.foreco.2014.05.018

Suzuki, Y., S.J. Grayston, & Prescott, C.E. (2013). Effects of leaf litter consumption by millipedes (Harpaphe haydeniana) on subsequent decomposition depends on litter type. Soil Biology and Biochemistry, 57, 116-123. https://doi.org/10.1016/j.soilbio.2012.07.020

Triplehorn, C.A. & N.F Johnson. (2005). Borror and DeLong’s lntroduction to the Study of lnsects. Thomson Brooks/Cole. 864 p.

Vohland, K., & Schroth, G. (1999). Distribution patterns of the litter macrofauna in agroforestry and monoculture plantations in Central Amazonia as affected by plant species and management. Applied Soil Ecology,13(1), 57-68. https://doi.org/10.1016/S0929-1393(99)00021-9

Voříšková, J., & Baldrian, P. (2013). Fungal community on decomposing leaf litter undergoes rapid successional changes. The ISME Journal, 7(3), 477-486. https://doi.org/10.1038/ismej.2012.116

Wardle, D.A., G.W. Yeates, G.M. Barker, & Bonner, K.I. (2006). The influence of plant litter diversity on decomposer abundance and diversity. Soil Biology and Biochemistry, 38(5), 1052-1062. https://doi.org/10.1016/j.soilbio.2005.09.003
Sistema OJS - Metabiblioteca |