Visual and chemical cues from aquatic snails reduce chironomid oviposition
Jacqueline S.-L. Devereaux A and Allie Mokany A B CA School of Botany and Zoology, Australian National University, Canberra, ACT 0200, Australia.
B CSIRO Entomology, Canberra, ACT 2601, Australia.
C Corresponding author. Email: allie.mokany@anu.edu.au
Australian Journal of Zoology 54(2) 79-86 https://doi.org/10.1071/ZO05069
Submitted: 7 November 2005 Accepted: 8 March 2006 Published: 11 May 2006
Abstract
Chironomus oppositus sensu lato and the freshwater gastropod Physa acuta are distantly related taxa inhabiting temporary ponds. Although their distributions overlap, their peak abundances do not coincide in time and space. This study used field-based mesocosm experiments to examine the effect of P. acuta on the distribution and abundance of C. oppositus. Results indicated that chironomid larval abundance was substantially higher in mesocosms without P. acuta. The abundance of C. oppositus decreased as snail density increased, from one snail per litre. To investigate whether this result was due to differential survival by chironomid larvae or preferential oviposition by chironomid adults, both factors were manipulated separately and the mechanisms involved investigated. Direct-interaction experiments demonstrated that direct (mechanical) and indirect (water-borne) interference by snails had limited impact on the survivorship of third- or fourth-instar C. oppositus. Oviposition trials indicated that chironomid egg strings were five times less abundant in mesocosms containing both visual and water-borne snail cues. However, the presence of each of these cues separately did not result in a similar reduction. This study demonstrates that negative covariance occurred between larval chironomids and snails, with chironomids avoiding snails through oviposition site selection. This has important implications for understanding the mechanisms structuring freshwater communities.
Acknowledgments
We are grateful for the guidance of Jeff Wood, Christine Donnelly and David Gordon in their statistical assistance. We also thank Jonathan Chase, Saul Cunningham, Mike Jennions, Jessica Stapley and Leon Blaustein for their valuable comments on drafts. Also thank you to Peter Cranston for identifying the chironomid species. The CSIRO provided financial support for this study.
Beehler, J. W. , Millar, J. G. , and Mulla, M. S. (1993). Synergism between chemical attractants and visual cues influencing oviposition of the mosquito, Culex quinquefasciatus (Diptera, Culicidae). Journal of Chemical Ecology 19, 635–644.
| Crossref | GoogleScholarGoogle Scholar |
Brönmark, C. , Rundle, S. D. , and Erlandsson, A. (1991). Interactions between fresh-water snails and tadpoles – competition and facilitation. Oecologia 87, 8–18.
| Crossref | GoogleScholarGoogle Scholar |
Connell, J. H. (1983). On the prevalence and relative importance of interspecific competition: evidence from field experiments. American Naturalist 122, 661–694.
| Crossref | GoogleScholarGoogle Scholar |
Gresens, S. E. (1995). Grazer diversity, competition and the response of the periphyton community. Oikos 73, 336–346.
McNaughton, S. J. (1977). Diversity and stability of ecological communities – comment on role of empiricism in ecology. American Naturalist 111, 515–525.
| Crossref | GoogleScholarGoogle Scholar |
Millar, J. G. , Chaney, J. D. , Beehler, J. W. , and Mulla, M. S. (1994). Interaction of the Culex quinquefasciatus egg raft pheromone with a natural chemical associated with oviposition sites. Journal of the American Mosquito Control Association 10, 374–379.
| PubMed |
Miller, T. E. , Burns, J. H. , Munguia, P. , Walters, E. L. , Kneitel, J. M. , Richards, P. M. , Mouquet, N. , and Buckley, H. L. (2005). A critical review of twenty years’ use of the resource-ratio theory. American Naturalis 165, 439–448.
| Crossref | GoogleScholarGoogle Scholar |
Mokany, A. , and Shine, R. (2002a). Competition between tadpoles and mosquitoes: the effects of larval density and tadpole size. Australian Journal of Zoology 50, 549–563.
| Crossref | GoogleScholarGoogle Scholar |
Mokany, A. , and Shine, R. (2002b). Pond attributes influence competitive interactions between tadpoles and mosquito larvae. Austral Ecology 27, 396–404.
| Crossref | GoogleScholarGoogle Scholar |
Mokany, A. , and Shine, R. (2003a). Biological warfare in the garden pond: tadpoles suppress the growth of mosquito larvae. Ecological Entomology 28, 102–108.
| Crossref | GoogleScholarGoogle Scholar |
Mokany, A. , and Shine, R. (2003b). Oviposition site selection by mosquitoes is affected by cues from conspecific larvae and anuran tadpoles. Austral Ecology 28, 33–37.
| Crossref | GoogleScholarGoogle Scholar |
Morin, P. J. , Lawler, S. P. , and Johnson, E. A. (1988). Competition between aquatic insects and vertebrates – interaction strength and higher-order interactions. Ecology 69, 1401–1409.
| Crossref | GoogleScholarGoogle Scholar |
Oliver, D. R. (1971). Life history of Chironomidae. Annual Review of Entomology 16, 211–230.
| Crossref | GoogleScholarGoogle Scholar |
Onyabe, D. Y. , and Roitberg, B. D. (1997). The effect of conspecifics on oviposition site selection and oviposition behaviour in Aedes togoi (Theobold) (Diptera: Culicidae). Canadian Entomologist 129, 1173–1176.
Petranka, J. W. , and Fakhoury, K. (1991). Evidence of a chemically-mediated avoidance-response of ovipositing insects to blue-gills and green frog tadpoles. Copeia 1, 234–239.
| Crossref | GoogleScholarGoogle Scholar |
Pinder, L. C. V. (1986). Biology of fresh-water Chironomidae. Annual Review of Entomology 31, 1–23.
Resetarits, W. J. , and Wilbur, H. M. (1989). Choice of oviposition site by Hyla chrysoscelis – role of predators and competitors. Ecology 70, 220–228.
| Crossref | GoogleScholarGoogle Scholar |
Richards, D. C. , and Shinn, D. C. (2004). Intraspecific competition and development of size structure in the invasive snail Potamopyrgus antipodarum (Gray, 1853). American Malacological Bulletin 19, 33–37.
Rohr, J. R. , and Crumrine, P. W. (2005). Effects of an herbicide and an insecticide on pond community structure and processes. Ecological Applications 15, 1135–1147.
Schmitt, R. J. (1996). Exploitation competition in mobile grazers: trade-offs in use of a limited resource. Ecology 77, 408–425.
| Crossref | GoogleScholarGoogle Scholar |
Spencer, M. , Blaustein, L. , and Cohen, J. E. (2002). Oviposition habitat selection by mosquitoes (Culiseta longiareolata) and consequences for population size. Ecology 83, 669–679.
Stav, G. , Blaustein, L. , and Margalit, Y. (2005). Individual and interactive effects of a predator and controphic species on mosquito populations. Ecological Applications 15, 587–598.
Stevens, M. M. , Warren, G. N. , and Braysher, B. D. (2003). Oviposition response of Chironomus tepperi to nitrogenous compounds and bioextracts in two-choice laboratory tests. Journal of Chemical Ecology 29, 911–920.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Tilman, D. , Lehman, C. L. , and Bristow, C. E. (1998). Diversity-stability relationships: statistical inevitability or ecological consequence? American Naturalist 151, 277–282.
| Crossref | GoogleScholarGoogle Scholar |
Tokeshi, M. (1995). Randomness and aggregation – analysis of dispersion in an epiphytic chironomid community. Freshwater Biology 33, 567–578.
Yachi, S. , and Loreau, M. (1999). Biodiversity and ecosystem productivity in a fluctuating environment: the insurance hypothesis. Proceedings of the National Academy of Sciences of the United States of America 96, 1463–1468.
| Crossref | GoogleScholarGoogle Scholar | PubMed |