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PeerJ  2015 

The role of a water bug, Sigara striata, in freshwater food webs

DOI: 10.7717/peerj.389

Keywords: Predation,Predator–prey interactions,Food webs,Foraging,Heteroptera,Corixidae

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Abstract:

Freshwater food webs are dominated by aquatic invertebrates whose trophic relationships are often poorly known. Here, I used laboratory experiments to study the role of a water bug, Sigara striata, as a potential predator and prey in food webs of stagnant waters. Multiple-choice predation experiment revealed that Sigara, which had been considered mostly herbivorous, also consumed larvae of Chironomus midges. Because they often occur in high densities and are among the most ubiquitous aquatic insects, Sigara water bugs may be important predators in fresh waters. A second experiment tested the role of Sigara as a potential prey for 13 common invertebrate predators. Mortality of Sigara inflicted by different predators varied widely, especially depending on body mass, foraging mode (ambush/searching) and feeding mode (chewing/suctorial) of the predators. Sigara was highly vulnerable to ambush predators, while searching predators caused on average 8.1 times lower mortality of Sigara. Additionally, suctorial predators consumed on average 6.6 times more Sigara individuals than chewing predators, which supports previous results hinting on potentially different predation pressures of these two types of predators on prey populations. The importance of these two foraging-related traits demonstrates the need to move from body mass based to multiple trait based descriptions of food web structure. Overall, the results suggests that detailed experimental studies of common but insufficiently known species can significantly enhance our understanding of food web structure.

References

[1]  Alahmed S, Alamr A, Kheir S. 2009. Seasonal activity and predatory efficacy of the water bug Sigara hoggarica Poisson (hemiptera: Corixidae) against the mosquito larvae Culex quinquefasciatus (diptera: Culicidae) in Riyadh City, Saudi Arabia. Journal of Entomology 6:90-95
[2]  Allan AS, Flecker J, McClintock N. 1987. Prey preference of stoneflies: sedentary vs. mobile prey. Oikos 49:323-331
[3]  Arnér M, Koivisto S, Norberg J, Kautsky N. 1998. Trophic interactions in rockpool food webs: regulation of zooplankton and phytoplankton by Notonecta and Daphnia. Freshwater Biology 39:79-90
[4]  Bascompte J, Jordano P. 2007. Plant-animal mutualistic networks: the architecture of biodiversity. Annual Review of Ecology, Evolution, and Systematics 38:567-593
[5]  Bascompte J, Jordano P, Melián C, Olesen J. 2003. The nested assembly of plant-animal mutualistic networks. Proceedings of the National Academy of Sciences of the United States of America 100:9383-9387
[6]  Beckerman A, Petchey O, Warren P. 2006. Foraging biology predicts food web complexity. Proceedings of the National Academy of Sciences of the United States of America 103:13745-13749
[7]  Bendell BE, McNicol DK. 1995. Lake acidity, fish predation, and the distribution and abundance of some littoral insects. Hydrobiologia 302:133-145
[8]  Boukal D, Boukal M, Fikacek M, Hajek J, Klecka J, Skalicky S, Stastny J, Travnicek D. 2007. Katalog vodních brouk eské republiky/catalogue of water beetles of the Czech Republic. Klapalekiana 43:1-289
[9]  Brose U, Jonsson T, Berlow E, Warren P, Banasek-Richter C, Bersier LF, Blanchard J, Brey T, Carpenter S, Blandenier MF, Cushing L, Dawah H, Dell T, Edwards F, Harper-Smith S, Jacob U, Ledger M, Martinez N, Memmott J, Mintenbeck K, Pinnegar J, Rall B, Rayner T, Reuman D, Ruess L, Ulrich W, Williams R, Woodward G, Cohen J. 2006. Consumer-resource body-size relationships in natural food webs. Ecology 87:2411-2417
[10]  Brose U, Williams R, Martinez N. 2006. Allometric scaling enhances stability in complex food webs. Ecology Letters 9:1228-1236
[11]  Cobbaert D, Bayley S, Greter JL. 2010. Effects of a top invertebrate predator (Dytiscus alaskanus; Coleoptera: Dytiscidae) on fishless pond ecosystems. Hydrobiologia 644:103-114
[12]  Cohen J, Briand F, Newman C. 1990. Community food webs: data and theory. Berlin: Springer.
[13]  Convey P. 1988. Competition for perches between larval damselflies: the influence of perch use on feeding efficiency, growth rate and predator avoidance. Freshwater Biology 19:15-28
[14]  Cooper S, Smith D, Bence J. 1985. Prey selection by freshwater predators with different foraging strategies. Canadian Journal of Fisheries and Aquatic Sciences 42:1720-1732
[15]  Culler L, Lamp W. 2009. Selective predation by larval Agabus (Coleoptera: Dytiscidae) on mosquitoes: support for conservation-based mosquito suppression in constructed wetlands. Freshwater Biology 54:2003-2014
[16]  de Ruiter P, Neutel AM, Moore J. 1995. Energetics, patterns of interaction strengths, and stability in real ecosystems. Science 269:1257-1260
[17]  Eklv P, Diehl S. 1994. Piscivore efficiency and refuging prey: the importance of predator search mode. Oecologia 98:344-353
[18]  Elton C. 1927. Animal ecology. New York: Macmillan Co.
[19]  Foltan P, Sheppard S, Konvicka M, Symondson WO. 2005. The significance of facultative scavenging in generalist predator nutrition: detecting decayed prey in the guts of predators using PCR. Molecular Ecology 14:4147-4158
[20]  Fortuna M, Bascompte J. 2006. Habitat loss and the structure of plant-animal mutualistic networks. Ecology Letters 9:278-283
[21]  Giller P. 1982. The natural diets of waterbugs (Hemiptera-Heteroptera): electrophoresis as a potential method of analysis. Ecological Entomology 7:233-237
[22]  Giller P. 1984. Predator gut state and prey detectability using electrophoretic analysis of gut contents. Ecological Entomology 9:157-162
[23]  Giller P. 1986. The natural diet of the Notonectidae: field trials using electrophoresis. Ecological Entomology 11:163-172
[24]  Gilljam D, Thierry A, Edwards F, Figueroa D, Ibbotson A, Jones J, Lauridsen R, Petchey O, Woodward G, Ebenman B. 2011. Seeing double: size-based and taxonomic views of food web structure. Advances in Ecological Research 45:67-133
[25]  Günther B, Rall BC, Ferlian O, Scheu S, Eitzinger B. Variations in prey consumption of centipede predators in forest soils as indicated by molecular gut content analysis. Oikos In press
[26]  Heckmann L, Drossel B, Brose U, Guill C. 2012. Interactive effects of body-size structure and adaptive foraging on food-web stability. Ecology Letters 15:243-250
[27]  Horinouchi M, Mizuno N, Jo Y, Fujita M, Sano M, Suzuki Y. 2009. Seagrass habitat complexity does not always decrease foraging efficiencies of piscivorous fishes. Marine Ecology Progress Series 377:43-49
[28]  Hutchinson G. 1993. A treatise on limnology, Vol. 4, The Zoobenthos. New York: Wiley & Sons.
[29]  Ings T, Montoya J, Bascompte J, Blüthgen N, Brown L, Dormann C, Edwards F, Figueroa D, Jacob U, Jones J, Lauridsen R, Ledger M, Lewis H, Olesen J, Van Veen F, Warren P, Woodward G. 2009. Ecological networks—beyond food webs. Journal of Animal Ecology 78:253-269
[30]  Klecka J, Boukal D. 2011. Lazy ecologist’s guide to water beetle diversity: Which sampling methods are the best? Ecological Indicators 11:500-508
[31]  Klecka J, Boukal D. 2012. Who eats whom in a pool? a comparative study of prey selectivity by predatory aquatic insects. PLoS ONE 7:e37741
[32]  Klecka J, Boukal D. 2013. Foraging and vulnerability traits modify predator–prey body mass allometry: freshwater macroinvertebrates as a case study. Journal of Animal Ecology 82:1031-1041
[33]  Layer K, Hildrew A, Monteith D, Woodward G. 2010. Long-term variation in the littoral food web of an acidified mountain lake. Global Change Biology 16:3133-3143
[34]  May RM. 1972. Will a large complex system be stable? Nature 238:413-414
[35]  McCann K, Hastings A, Huxel G. 1998. Weak trophic interactions and the balance of nature. Nature 395:794-798
[36]  Melián C, Bascompte J. 2002. Food web structure and habitat loss. Ecology Letters 5:37-46
[37]  Melián C, Vilas C, Baldó F, González-Ortegón E, Drake P, Williams R. 2011. Eco-evolutionary dynamics of individual-based food webs. Advances in Ecological Research 45:225-268
[38]  Michel MJ, Adams MM. 2009. Differential effects of structural complexity on predator foraging behavior. Behavioral Ecology 20:313-317
[39]  Morales ME, Wesson DM, Sutherland IW, Impoinvil DE, Mbogo CM, Githure JI, Beier JC. 2003. Determination of Anopheles gambiae larval DNA in the gut of insectivorous dragonfly (libellulidae) nymphs by polymerase chain reaction. Journal of the American Mosquito Control Association 19:163-165
[40]  Nakazawa T, Ohba Sy, Ushio M. 2013. Predator–prey body size relationships when predators can consume prey larger than themselves. Biology Letters 9:20121193
[41]  O’Gorman E, Pichler D, Adams G, Benstead J, Cohen H, Craig N, Cross W, Demars B, Friberg N, Gislason G, Gudmundsdottir R, Hawczak A, Hood J, Hudson L, Johansson L, Johansson M, Junker J, Laurila A, Manson J, Mavromati E, Nelson D, Olafsson J, Perkins D, Petchey O, Plebani M, Reuman D, Rall B, Stewart R, Thompson M, Woodward G. 2012. Impacts of warming on the structure and functioning of aquatic communities. individual- to ecosystem-level responses. Advances in Ecological Research 47:81-176
[42]  Ohba SY, Kawada H, Dida GO, Juma D, Sonye G, Minakawa N, Takagi M. 2010. Predators of Anopheles gambiae sensu lato (Diptera: Culicidae) larvae in wetlands, western Kenya: confirmation by polymerase chain reaction method. Journal of Medical Entomology 47:783-787
[43]  Peckarsky BL. 1982. Aquatic insect predator–prey relations. BioScience 32:261-266
[44]  Petchey O, Beckerman A, Riede J, Warren P. 2008. Size, foraging, and food web structure. Proceedings of the National Academy of Sciences of the United States of America 105:4191-4196
[45]  Petchey O, Brose U, Rall B. 2010. Predicting the effects of temperature on food web connectance. Philosophical Transactions of the Royal Society B: Biological Sciences 365:2081-2091
[46]  Plummer M. 2003. Jags: a program for analysis of Bayesian graphical models using Gibbs sampling. In: Hornik K, Leisch F, Zeileis A, eds. Proceedings of the 3rd International Workshop on Distributed Statistical Computing, Vienna, Austria. Available at http://www.r-project.org/conferences/DSC-2003/Proceedings/Plummer.pdf (accessed 1 February 2014)
[47]  Plummer M. 2013. rjags: Bayesian graphical models using MCMC (R package version 3-11). Available at http://CRAN.R-project.org/package=rjags
[48]  Plummer M, Best N, Cowles K, Vines K. 2006. Coda: convergence diagnosis and output analysis for mcmc. R News 6:7-11 Available at http://CRAN.R-project.org/doc/Rnews/
[49]  Polis G. 1991. Complex trophic interactions in deserts: an empirical critique of food-web theory. American Naturalist 138:123-155
[50]  Pompanon F, Deagle BE, Symondson WO, Brown DS, Jarman SN, Taberlet P. 2012. Who is eating what: diet assessment using next generation sequencing. Molecular Ecology 21:1931-1950
[51]  Popham EJ, Bryant MT, Savage AA. 1984. The role of front legs of british corixid bugs in feeding and mating. Journal of Natural History 18:445-464
[52]  R Core Team. 2013. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing. Available at http://www.R-project.org/
[53]  Rohr R, Scherer H, Kehrli P, Mazza C, Bersier LF. 2010. Modeling food webs: exploring unexplained structure using latent traits. American Naturalist 176:170-177
[54]  Rossberg A, Brnnstrm , Dieckmann U. 2010. How trophic interaction strength depends on traits. Theoretical Ecology 3:13-24
[55]  Schilling EG, Loftin CS, Huryn AD. 2009. Macroinvertebrates as indicators of fish absence in naturally fishless lakes. Freshwater Biology 54:181-202
[56]  Shaalan ES, Canyon D. 2009. Aquatic insect predators and mosquito control. Tropical Biomedicine 26:223-261
[57]  Symondson W. 2002. Molecular identification of prey in predator diets. Molecular Ecology 11:627-641
[58]  Tate AW, Hershey AE. 2003. Selective feeding by larval dytiscids (Coleoptera: Dytiscidae) and effects of fish predation on upper littoral zone macroinvertebrate communities of arctic lakes. Hydrobiologia 497:13-23
[59]  Thompson R, Dunne J, Woodward G. 2012. Freshwater food webs: towards a more fundamental understanding of biodiversity and community dynamics. Freshwater Biology 57:1329-1341
[60]  Tolonen K, Hmlinen H, Holopainen I, Mikkonen K, Karjalainen J. 2003. Body size and substrate association of littoral insects in relation to vegetation structure. Hydrobiologia 499:179-190
[61]  Warren P. 1989. Spatial and temporal variation in the structure of a freshwater food web. Oikos 55:299-311
[62]  Williams R, Anandanadesan A, Purves D. 2010. The probabilistic niche model reveals the niche structure and role of body size in a complex food web. PLoS ONE 5:e12092
[63]  Williams R, Purves D. 2011. The probabilistic niche model reveals substantial variation in the niche structure of empirical food webs. Ecology 92:1849-1857
[64]  Wirtz K. 2012. Who is eating whom? morphology and feeding type determine the size relation between planktonic predators and their ideal prey. Marine Ecology Progress Series 445:1-12
[65]  Woodward G, Hildrew A. 2002. Body-size determinants of niche overlap and intraguild predation within a complex food web. Journal of Animal Ecology 71:1063-1074
[66]  Wootton JT. 1997. Estimates and tests of per capita interaction strength: diet, abundance, and impact of intertidally foraging birds. Ecological Monographs 67:45-64

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