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Effects of combination of leaf resources on competition in container mosquito larvae

Published online by Cambridge University Press:  07 February 2012

M.H. Reiskind*
Affiliation:
Department of Entomology and Plant Pathology, 127 Noble Research Center, Oklahoma State University, Stillwater, OK 74078, USA
A.A. Zarrabi
Affiliation:
Department of Entomology and Plant Pathology, 127 Noble Research Center, Oklahoma State University, Stillwater, OK 74078, USA
L.P. Lounibos
Affiliation:
Florida Medical Entomology Laboratory, Department of Entomology and Nematology, University of Florida, 200 9th Street SE, Vero Beach, FL 32962, USA
*
*Author for correspondence Fax: 01-(405)-744-6039 E-mail: michael.h.reiskind@okstate.edu

Abstract

Resource diversity is critical to fitness in many insect species, and may determine the coexistence of competitive species and the function of ecosystems. Plant material provides the nutritional base for numerous aquatic systems, yet the consequences of diversity of plant material have not been studied in aquatic container systems important for the production of mosquitoes. To address how diversity in leaf detritus affects container-inhabiting mosquitoes, we examined how leaf species affect competition between two container inhabiting mosquito larvae, Aedes aegypti and Aedes albopictus, that co-occur in many parts of the world. We tested the hypotheses that leaf species changes the outcome of intra- and interspecific competition between these mosquito species, and that combinations of leaf species affect competition in a manner not predictable based upon the response to each leaf species alone (i.e. the response to leaf combinations is non-additive). We find support for our first hypothesis that leaf species can affect competition, evidence that, in general, leaf combination alters competitive interactions, and no support that leaf combination impacts interspecific competition differently than intraspecific competition. We conclude that combinations of leaves increase mosquito production non-additively such that combinations of leaves act synergistically, in general, and result in higher total yield of adult mosquitoes in most cases, although certain leaf combinations for A. albopictus are antagonistic. We also conclude that leaf diversity does not have a different effect on interspecific competition between A. aegypti and A. albopictus, relative to intraspecific competition for each mosquito.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 2012

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References

Ball, B.A., Hunter, M.D., Kominoski, J.S., Swan, C.M. & Bradford, M.A. (2008) Consequences of non-random species loss for decomposition dynamics: experimental evidence for additive and non-additive effects. Journal of Ecology 96, 303313.Google Scholar
Barrera, R. (1996) Competition and resistance to starvation in larvae of container-inhabiting Aedes mosquitoes. Ecological Entomology 21, 117127.CrossRefGoogle Scholar
Barrera, R., Amador, M. & Clark, G.G. (2006) Ecological factors influencing Aedes aegypti (Diptera : Culicidae) productivity in artificial containers in Salinas, Puerto Rico. Journal of Medical Entomology 43, 484492.Google Scholar
Behmer, S.T. (2009) Insect herbivore nutrient regulation. Annual Review of Entomology 54, 165187.Google Scholar
Behmer, S.T. & Joern, A. (2008) Coexisting generalist herbivores occupy unique nutritional feeding niches. Proceedings of the National Academy of Sciences of the United States of America 105, 19771982.Google Scholar
Braks, M.A.H., Honorio, N.A., Lounibos, L.P., Lourenco-De-Oliveira, R. & Juliano, S.A. (2004) Interspecific competition between two invasive species of container mosquitoes, Aedes aegypti and Aedes albopictus (Diptera: Culicidae), in Brazil. Annals of the Entomological Society of America 97, 130139.Google Scholar
Cardinale, B.J., Bennett, D.M., Nelson, C.E. & Gross, K. (2009) Does productivity drive diversity or vice versa? A test of the multivariate productivity-diversity hypothesis in streams. Ecology 90, 12271241.CrossRefGoogle ScholarPubMed
Christophers, S.R. (1960) Aëdes aegypti (L.). The Yellow Fever Mosquito; Its Life History, Bionomics, and Structure. Cambridge, UK, University Press.Google Scholar
Dadd, R.H. (1970) Relationship between filtering activity and ingestion of solids by larvae of mosquito Culex-pipiens: a method for assessing phagostimulant factors. Journal of Medical Entomology 7, 708712.Google Scholar
Daugherty, M.P., Alto, B.W. & Juliano, S.A. (2000) Invertebrate carcasses as a resource for competing Aedes albopictus and Aedes aegypti (Diptera: Culicidae). Journal of Medical Entomology 37, 364372.CrossRefGoogle ScholarPubMed
David, J.P., Rey, D., Cuany, A., Amichot, M. & Meyran, J.C. (2000a) Comparative ability to detoxify alder leaf litter in field larval mosquito collections. Archives of Insect Biochemistry and Physiology 44, 143150.Google Scholar
David, J.P., Rey, D., Pautou, M.P. & Meyran, J.C. (2000b) Differential toxicity of leaf litter to dipteran larvae of mosquito developmental sites. Journal of Invertebrate Pathology 75, 918.Google Scholar
David, J.P., Tilquin, M., Rey, D., Ravanel, P. & Meyran, J.C. (2003) Mosquito larval consumption of toxic arborescent leaf-litter, and its biocontrol potential. Medical and Veterinary Entomology 17, 151157.Google Scholar
Dieng, H., Mwandawiro, C., Boots, M., Morales, R., Satho, T., Tuno, N., Tsuda, Y. & Takagi, M. (2002) Leaf litter decay process and the growth performance of Aedes albopictus larvae (Diptera: Culicidae). Journal of Vector Ecology 27, 3138.Google Scholar
Elser, J.J., Marzolf, E.R. & Goldman, C.R. (1990) Phosphorus and nitrogen limitation of phytoplankton growth in the fresh-waters of north-america: a review and critique of experimental enrichments. Canadian Journal of Fisheries and Aquatic Sciences 47, 14681477.Google Scholar
Eubanks, M.D. & Denno, R.F. (1999) The ecological consequences of variation in plants and prey for an omnivorous insect. Ecology 80, 12531266.CrossRefGoogle Scholar
Fish, D. & Carpenter, S.R. (1982) Leaf litter and larval mosquito dynamics in tree-hole ecosystems. Ecology 63, 283288.CrossRefGoogle Scholar
Frost, P.C., Stelzer, R.S., Lamberti, G.A. & Elser, J.J. (2002) Ecological stoichiometry of trophic interactions in the benthos: understanding the role of C:N:P ratios in lentic and lotic habitats. Journal of the North American Benthological Society 21, 515528.Google Scholar
Gilpin, M.E., McClelland, G.A.H. & Pearson, J.W. (1976) Space, time, and stability of laboratory mosquito populations. American Naturalist 110, 11071111.CrossRefGoogle Scholar
Greenstone, M.H. (1979) Spider feeding-behavior optimizes dietary essential amino-acid composition. Nature 282, 501503.Google Scholar
Hattenschwiler, S., Tiunov, A.V. & Scheu, S. (2005) Biodiversity and litter decomposition interrestrial ecosystems. Annual Review of Ecology Evolution and Systematics 36, 191218.Google Scholar
Hawley, W. (1988) The biology of Aedes albopictus. Journal of the American Mosquito Control Association Supplement 1, 140.Google Scholar
Huston, M.A. (1997) Hidden treatments in ecological experiments: re-evaluating the ecosystem function of biodiversity. Oecologia 110, 449460.CrossRefGoogle ScholarPubMed
Hutchinson, G.E. (1959) Homage to Santa-Rosalia or why are there so many kinds of animals. American Naturalist 93, 145159.Google Scholar
Inouye, B.D. (2001) Response surface experimental designs for investigating interspecific competition. Ecology 82, 26962706.Google Scholar
Juliano, S.A. (1998) Species introduction and replacement among mosquitoes: Interspecific resource competition or apparent competition? Ecology 79, 255268.CrossRefGoogle Scholar
Juliano, S.A. (2007) Population dynamics. Journal of the American Mosquito Control Association 23, 265275.Google Scholar
Juliano, S.A. (2009) Species interactions among larval mosquitoes: context dependence across habitat gradients. Annual Review of Entomology 54, 3756.Google Scholar
Juliano, S.A. (2010) Coexistence, exclusion, or neutrality? A meta-analysis of competition between Aedes albopictus and resident mosquitoes. Israeli Journal of Ecology and Evolution 56, 325361.CrossRefGoogle ScholarPubMed
Kaspari, M. & Yanoviak, S.P. (2009) Biogeochemistry and the structure of tropical brown food webs. Ecology 90, 33423351.CrossRefGoogle ScholarPubMed
Kaspari, M., Yanoviak, S.P. & Dudley, R. (2008) On the biogeography of salt limitation: a study of ant communities. Proceedings of the National Academy of Sciences of the United States of America 105, 1784817851.Google Scholar
Kaufman, M.G., Goodfriend, W., Kohler-Garrigan, A., Walker, E.D. & Klug, M.J. (2002) Soluble nutrient effects on microbial communities and mosquito production in Ochlerotatus triseriatus habitats. Aquatic Microbial Ecology 29, 7388.Google Scholar
Lehman, J.T. (1976) Filter-feeder as an optimal forager, and predicted shapes of feeding curves. Limnology and Oceanography 21, 501516.Google Scholar
Loreau, M., Naeem, S., Inchausti, P., Bengtsson, J., Grime, J.P., Hector, A., Hooper, D.U., Huston, M.A., Raffaelli, D., Schmid, B., Tilman, D. & Wardle, D.A. (2001) Ecology – Biodiversity and ecosystem functioning: current knowledge and future challenges. Science 294, 804808.Google Scholar
Merritt, R.W., Dadd, R.H. & Walker, E.D. (1992) Feeding-behavior, natural food, and nutritional relationships of larval mosquitos. Annual Review of Entomology 37, 349376.Google Scholar
Mittelbach, G.G., Steiner, C.F., Scheiner, S.M., Gross, K.L., Reynolds, H.L., Waide, R.B., Willig, M.R., Dodson, S.I. & Gough, L. (2001) What is the observed relationship between species richness and productivity? Ecology 82, 23812396.CrossRefGoogle Scholar
Murrell, E.G. & Juliano, S.A. (2008) Detritus type alters the outcome of interspecific competition between Aedes aegypti and Aedes albopictus (Diptera: Culicidae). Journal of Medical Entomology 45, 375383.Google Scholar
O'Meara, G.F., Evans, L.F., Gettman, A.D. & Cuda, J.P. (1995) Spread of Aedes-albopictus and decline of Aedes-aegypti (Diptera, Culicidae) in Florida. Journal of Medical Entomology 32, 554562.CrossRefGoogle ScholarPubMed
Ponnusamy, L., Xu, N., Nojima, S., Wesson, D.M., Schal, C. & Apperson, C.S. (2008) Identification of bacteria and bacteria-associated chemical cues that mediate oviposition site preferences by Aedes aegypti. Proceedings of the National Academy of Sciences of the United States of America 105, 92629267.CrossRefGoogle ScholarPubMed
Pyke, G.H. (1984) Optimal foraging theory: a critical-review. Annual Review of Ecology and Systematics 15, 523575.Google Scholar
Reiskind, M.H., Greene, K.L. & Lounibos, L.P. (2009) Leaf species identity and combination affect performance and oviposition choice of two container mosquito species. Ecological Entomology 34, 447456.Google Scholar
Reiskind, M.H., Zarrabi, A.A. & Lounibos, L.P. (2010) Invasive leaf resources alleviate density dependence in the invasive mosquito, Aedes albopictus. Biological Invasions 12, 23192328.CrossRefGoogle ScholarPubMed
Scheiner, S.M. & Gurevitch, J. (2001) Design and Analysis of Ecological Experiments. 2nd edn.Oxford, UK, Oxford University Press.Google Scholar
Smith, V.C. & Bradford, M.A. (2003) Do non-additive effects on decomposition in litter-mix experiments result from differences in resource quality between litters? Oikos 102, 235242.Google Scholar
Sota, T. (1993) Performance of Aedes-albopictus and A-riversi larvae (Diptera, Culicidae) in waters that contain tannic-acid and decaying leaves: is the treehole species better adapted to treehole water. Annals of the Entomological Society of America 86, 450457.CrossRefGoogle Scholar
Srivastava, D.S., Cardinale, B.J., Downing, A.L., Duffy, J.E., Jouseau, C., Sankaran, M. & Wright, J.P. (2009) Diversity has stronger top-down than bottom-up effects on decomposition. Ecology 90, 10731083.Google Scholar
Swan, C.M. & Palmer, M.A. (2006) Composition of speciose leaf litter alters stream detritivore growth, feeding activity and leaf breakdown. Oecologia 147, 469478.Google Scholar
Swan, C.M., Gluth, M.A. & Horne, C.L. (2009) Leaf litter species evenness influences nonadditive breakdown in a headwater stream. Ecology 90, 16501658.Google Scholar
Tilman, D. (1980) Resources: a graphical-mechanistic approach to competition and predation. American Naturalist 116, 362393.CrossRefGoogle Scholar
Tilman, D., Wedin, D. & Knops, J. (1996) Productivity and sustainability influenced by biodiversity in grassland ecosystems. Nature 379, 718720.CrossRefGoogle Scholar
Vitousek, P.M. & Howarth, R.W. (1991) Nitrogen limitation on land and in the sea: how can it occur? Biogeochemistry 13, 87115.CrossRefGoogle Scholar
Waldbauer, G.P. & Friedman, S. (1991) Self-selection of optimal diets by insects. Annual Review of Entomology 36, 4363.CrossRefGoogle Scholar
Walker, E.D. & Merritt, R.W. (1988) The significance of leaf detritus to mosquito (diptera, culicidae) productivity from treeholes. Environmental Entomology 17, 199206.CrossRefGoogle Scholar
Walker, E.D., Olds, E.J. & Merritt, R.W. (1988) Gut content-analysis of mosquito larvae (Diptera, Culicidae) using dapi stain and epifluorescence microscopy. Journal of Medical Entomology 25, 551554.Google Scholar
Walker, E.D., Lawson, D.L., Merritt, R.W., Morgan, W.T. & Klug, M.J. (1991) Nutrient dynamics, bacterial-populations, and mosquito productivity in tree hole ecosystems and microcosms. Ecology 72, 15291546.Google Scholar
Yanoviak, S.P. (1999) Effects of leaf litter species on macroinvertebrate community properties and mosquito yield in Neotropical tree hole microcosms. Oecologia 120, 147155.Google Scholar
Yee, D.A. & Juliano, S.A. (2006) Consequences of detritus type in an aquatic microsystem: effects on water quality, micro-organisms and performance of the dominant consumer. Freshwater Biology 51, 448459.Google Scholar
Yee, D.A., Kaufman, M.G. & Juliano, S.A. (2007) The significance of ratios of detritus types and micro-organism productivity to competitive interactions between aquatic insect detritivores. Journal of Animal Ecology 76, 11051115.CrossRefGoogle ScholarPubMed