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6 - Sociality in Aphids and Thrips

from Part I - Invertebrates

Published online by Cambridge University Press:  13 April 2017

By
Patrick Abbot  and
Tom Chapman
Edited by
Dustin R. Rubenstein  and
Patrick Abbot
Dustin R. Rubenstein
Affiliation:
Columbia University, New York
Patrick Abbot
Affiliation:
Vanderbilt University, Tennessee
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Comparative Social Evolution , pp. 154 - 187
Publisher: Cambridge University Press
Print publication year: 2017

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References

Abbot, P. (2009) On the evolution of dispersal and altruism in aphids. Evolution, 63, 2687–2696.CrossRefGoogle ScholarPubMed
Abbot, P. (2011) A closer look at the spatial architecture of aphid clones. Molecular Ecology, 20, 4587–4589.CrossRefGoogle Scholar
Abbot, P. (2015) The physiology and genomics of social transitions in aphids. In: Zayed, A. & Kent, C.F. (eds.) Genomics, Physiology and Behavior of Social Insects. Advances in Insect Physiology, Volume 48. New York: Academic Press, pp. 163–188.Google Scholar
Abbot, P. & Chhatre, V. (2007) Kin structure provides no explanation for intruders in social aphids. Molecular Ecology, 16, 3659–3670.CrossRefGoogle ScholarPubMed
Abbot, P. & Withgott, J. H. (2004) Phylogenetic and molecular evidence for allochronic speciation in gall-forming aphids (Pemphigus). Evolution, 58, 539–553.Google ScholarPubMed
Abbot, P., Withgott, J. H., & Moran, N. A. (2001) Genetic conflict and conditional altruism in social aphid colonies. Proceedings of the National Academy of Sciences of the United States of America, 98, 12068–12071.CrossRefGoogle ScholarPubMed
Akimoto, S. (1989) Gall-invading behavior of Eriosoma aphids (Homoptera, Pemphigidae) and its significance. Japanese Journal of Entomology, 57, 210–220.Google Scholar
Akimoto, S. (1996) Ecological factors promoting the evolution of colony defense in aphids: Computer simulations. Insectes Sociaux, 43, 1–15.CrossRefGoogle Scholar
Akimoto, S., & Yamaguchi, Y. (1997) Gall usurpation by the gall-forming aphid, Tetraneura sorini (Insecta Homoptera). Ethology Ecology and Evolution, 9, 159–168.CrossRefGoogle Scholar
Alexander, R. D., Noonan, K. M., & Crespi, B. J. (1991) The evolution of eusociality. In: Sherman, P.W., Jarvis, J. U. M., & Alexander, R.D. (eds.) The Biology of the Naked Mole Rat. Princeton: Princeton University Press, pp. 3–44.Google Scholar
Alton, K. (1999) The biology of Pemphigus spyrothecae galls on poplar leaves. PhD thesis, Nottingham: University of Nottingham.Google Scholar
Aoki, S. (1976) Occurrence of dimorphism in the first instar larva of Colophina clematis (Homoptera, Aphidoidea) Kontyû, 44, 130–137.Google Scholar
Aoki, S. (1979) Dimorphic first instar larvae produced by the fundatrix of Pachypappa marsupialis (Homoptera: Aphidoidea) Kontyû, 47, 390–398.Google Scholar
Aoki, S. & Kurosu, U. (2004) How many soldiers are optimal for an aphid colony? Journal of Theoretical Biology, 230, 313–317.CrossRefGoogle ScholarPubMed
Aoki, S. & Kurosu, U. (2010) A review of the biology of Cerataphidini (Hemiptera, Aphididae, Hormaphidinae), focusing mainly on their life cycles, gall formation, and soldiers. Psyche: A Journal of Entomology, 2010, 1–34.CrossRefGoogle Scholar
Aoki, S., Yamane, S., & Kiuchi, M. (1977) On the biters of Astegopteryx styracicola (Homoptera, Aphidoidea). Kontyû, 45, 563–570.Google Scholar
Aoki, S., Kurosu, U., & Stern, D. L. (1991) Aphid soldiers discriminate between soldiers and non-soldiers, rather than between kin and non-kin, in Ceratoglyphina bambusae. Animal Behaviour, 42, 865–866.CrossRefGoogle Scholar
Aoki, S., Kurosu, U., & Buranapanichpan, S. (2007) Female production within the gall and male production on leaves by individual alates of a social aphid. Insectes Sociaux, 54, 356–362.CrossRefGoogle Scholar
Benton, T. G. & Foster, W. A. (1992) Altruistic housekeeping in a social aphid. Proceedings of the Royal Society of London. Series B: Biological Sciences, 247, 199–202.Google Scholar
Blackman, R. L. & Eastop, V. F. (1994) Aphids on the World’s Trees: An Identification and Information Guide. London: University Press.CrossRefGoogle Scholar
Boomsma, J. J., Huszár, D. B., & Pedersen, J. S. (2014) The evolution of multiqueen breeding in eusocial lineages with permanent physically differentiated castes. Animal Behaviour, 92, 241–252.CrossRefGoogle Scholar
Bono, J. M. (2007) Patterns of kleptoparasitism and inquilinism in social and non-social Dunatothrips on Australian Acacia. Ecological Entomology, 32, 411–418.CrossRefGoogle Scholar
Bono, J. M. & Crespi, B. J. (2006) Costs and benefits of joint colony founding in Australian Acacia thrips. Insectes Sociaux, 53, 489–495.CrossRefGoogle Scholar
Bono, J. M. & Crespi, B. J. (2008) Cofoundress relatedness and group productivity in colonies of social Dunatothrips (Insecta: Thysanoptera) on Australian Acacia. Behavioral Ecology and Sociobiology, 62, 1489–1498.CrossRefGoogle ScholarPubMed
Cappuccino, N. (1987) Comparative population dynamics of two goldenrod aphids: Spatial patterns and temporal constancy. Ecology, 68, 1634–1646.CrossRefGoogle ScholarPubMed
Chapman, T. W. & Crespi, B. J. (1998) High relatedness and inbreeding in two species of haplodiploid eusocial thrips (Insecta: Thysanoptera) revealed by microsatellite analysis. Behavioral Ecology and Sociobiology, 43, 301–306.CrossRefGoogle Scholar
Chapman, T. W. & Perry, S. P. (2006) Evolution of fighting ability in soldiers of Australian gall thrips. In: Kipyatkov, V. (ed.) Life Cycles in Social Insects: Behaviour, Ecology and Evolution. St. Petersburg: St. Petersburg University Press, pp. 113–120.Google Scholar
Chapman, T. W., Crespi, B. J., Kranz, B. D., & Schwarz, M. P. (2000) High relatedness and inbreeding at the origin of eusociality in gall-inducing thrips. Proceedings of the National Academy of Sciences of the United States of America, 97, 1648–1650.CrossRefGoogle ScholarPubMed
Chapman, T. W., Kranz, B. D., Bejah, K. L., & Crespi, B. J. (2002) The evolution of soldier reproduction in social thrips. Behavioral Ecology, 13, 519–525.CrossRefGoogle Scholar
Chapman, T. W., Geyer, K. F., & Schwarz, M. P. (2006) The impact of kleptoparasitic invasions on the evolution of gall-size in social and solitary Australian Acacia thrips. Insect Science, 13, 391–400.CrossRefGoogle Scholar
Chapman, T. W., Crespi, B. J., & Perry, S. P. (2008) The evolutionary ecology of eusociality in Australian gall thrips: A “model clades” approach. In: Korb, J. & Heinze, J. (eds.) Ecology of Social Evolution. Berlin: Springer-Verlag, pp. 57–83.CrossRefGoogle Scholar
Childers, C. C., Beshear, R. J., Frantz, G., & Nelms, M. (2005) A review of thrips species biting man including records in Florida and Georgia between 1986–1997. Florida Entomologist, 88, 447–451.CrossRefGoogle Scholar
Choe, J. C. & Crespi, B. J. (1997) The Evolution of Social Behavior in Insects and Arachnids. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Clutton-Brock, T. (2009) Cooperation between non-kin in animal societies. Nature, 462, 51–57.CrossRefGoogle ScholarPubMed
Costa, J. T. (2006) The Other Social Insect Societies. Cambridge, MA: Harvard University Press.Google Scholar
Costa, J. T. & Fitzgerald, T. D. (2005) Social terminology revisited: Where are we ten years later? Annales Zoologici Fennici, 2, 559–564.Google Scholar
Crespi, B. J. (1986) Territoriality & fighting in a colonial thrips, Hoplothrips pedicularius, and sexual dimorphism in Thysanoptera. Ecological Entomology, 11, 119–130.CrossRefGoogle Scholar
Crespi, B. J. (1988) Alternative male mating tactics in a thrips: Effects of sex ratio variation and body size. American Midland Naturalist, 119, 83–92.CrossRefGoogle Scholar
Crespi, B. J. (1992a) Eusociality in Australian gall thrips. Nature, 359, 724–726.CrossRefGoogle Scholar
Crespi, B. J. (1992b) Behavioral ecology of Australian gall thrips (Insecta, Thysanoptera). Journal of Natural History, 26, 769–809.CrossRefGoogle Scholar
Crespi, B. J. (1994) Three conditions for the evolution of eusociality: are they sufficient? Insectes Sociaux, 41, 395–400.CrossRefGoogle Scholar
Crespi, B. J. (1996) Comparative analysis of the origins and losses of eusociality: Causal mosaics and historical uniqueness. In: Martins, E. (ed.) Phylogenies and the Comparative Method in Animal Behavior. Oxford: Oxford University Press, pp. 253–287.CrossRefGoogle Scholar
Crespi, B. J. & Abbot, P. (1999) The behavioral ecology and evolution of kleptoparasitism in Australian gall thrips. The Florida Entomologist, 82, 147.CrossRefGoogle Scholar
Crespi, B. J. & Worobey, M. (1998) Comparative analysis of gall morphology in Australian gall thrips: The evolution of extended phenotypes. Evolution, 52, 1686.CrossRefGoogle ScholarPubMed
Crespi, B. J. & Yanega, D. (1995) The definition of eusociality. Behavioral Ecology, 6: 109–115.CrossRefGoogle Scholar
Crespi, B. J., Carmean, D. A., & Chapman, T. W. (1997) Ecology and evolution of galling thrips and their allies. Annual Review Of Entomology, 42, 51–71.CrossRefGoogle ScholarPubMed
Crespi, B. J., Carmean, D. A., Mound, L. A., & Worobey, M. (1998) Phylogenetics of social behavior in Australian gall-forming thrips: Evidence from mitochondrial DNA sequence, adult morphology and behavior, and gall morphology. Molecular Phylogenetics and Evolution, 9, 163–180.CrossRefGoogle ScholarPubMed
Crespi, B. J., Morris, D. C., & Mound, L. A. (2004) Evolution of ecological and behavioral diversity: Australian Acacia thrips as model organisms. CSIRO, Canberra: Australian Biological Resources Study & Australian National Insect Collection.Google Scholar
de Bruijn, P. J. A. & Egas, M. (2014) Effects of kinship or familiarity? Small thrips larvae experience lower predation risk only in groups of mixed-size siblings. Behavioral Ecology and Sociobiology, 68, 1029–1035.Google ScholarPubMed
De Facci, M., Svensson, G. P., Chapman, T. W., & Anderbrant, O. (2013) Evidence for caste differences in anal droplet alarm pheromone production and responses in the eusocial thrips Kladothrips intermedius. Ethology, 119, 1118–1125.CrossRefGoogle Scholar
De Facci, M., Wang, H-L., Yuvaraj, J. K., et al. (2014) Chemical composition of anal droplets of the eusocial gall-inducing thrips Kladothrips intermedius. Chemoecology, 24, 85–94.CrossRefGoogle Scholar
de Kogel, W. J., Bosco, D., Van der Hoek, M., & Mollema, C. (1999) Effect of host plant on body size of Frankliniella occidentalis (Thysanoptera: Thripidae) and its correlation with reproductive capacity. European Journal of Entomology, 96, 365–368.Google Scholar
Dixon, A. F. G. (1998) Aphid Ecology. 2nd Edn. London: Chapman & Hall.Google Scholar
Emlen, S. T. (1982) The evolution of helping. I. An ecological constraints model. American Naturalist, 119, 29–39.CrossRefGoogle Scholar
Fernandes, G. W. & Price, P. W. (1988) Biogeographical gradients in galling species richness. Oecologia, 76, 161–167.CrossRefGoogle ScholarPubMed
Foster, W. A. (1990) Experimental evidence for effective and altruistic colony defense against natural predators by soldiers of the gall-forming aphid Pemphigus spyrothecae (Hemiptera: Pemphigidae). Behavioral Ecology and Sociobiology 27, 421–430.CrossRefGoogle Scholar
Foster, W. A. (1996) Duelling aphids: Intraspecific fighting in Astegopteryx minuta (Homoptera: Hormaphididae). Animal Behavior, 51, 645–655.CrossRefGoogle Scholar
Foster, W. A. (2009) Aphid sex ratios. In: Hardy, I.C.W. (ed.) Sex Ratios Concepts and Research Methods. Cambridge: Cambridge University Press, pp. 254–265.Google Scholar
Foster, W. A. & Benton, T. G. (1992) Sex ratio, local mate competition and mating behavior in the aphid Pemphigus spyrothecae. Behavioral Ecology and Sociobiology, 30, 297–307.CrossRefGoogle Scholar
Foster, W. A., & Northcott, N. A. (1994) Galls and the evolution of social behavior in aphids. In: Williams, M.A.J. (ed.) Plant Galls: Organisms, Interactions, Populations. Oxford: Oxford University Press, pp. 161–182.CrossRefGoogle Scholar
Foster, W. A. & Rhoden, P. (1998) Soldiers effectively defend aphid colonies against predators in the field. Animal Behaviour, 55, 761–765.CrossRefGoogle ScholarPubMed
Gilbert, J. D. J. (2014) Thrips domiciles protect larvae from desiccation in an arid environment. Behavioral Ecology, 25, 1338–1346.CrossRefGoogle Scholar
Gilbert, J. D. J. & Mound, L. A. (2012) Biology of a new species of socially parasitic thrips (Thysanoptera: Phlaeothripidae) inside Dunatothrips nests, with evolutionary implications for inquilinism in thrips. Biological Journal of the Linnean Society, 107, 112–122.CrossRefGoogle Scholar
Gilbert, J. D. J. & Simpson, S. J. (2013) Natural history and behavior of Dunatothrips aneurae Mound (Thysanoptera: Phlaeothripidae), a phyllode-gluing thrips with facultative pleometrosis. Biological Journal of the Linnean Society, 109, 802–816.CrossRefGoogle Scholar
Gonsalves, G. (2010) Host exploitation and fidelity in Acacia gall-invading parasites. Masters thesis, Memorial University of Newfoundland. Newfoundland: St. Johns.Google Scholar
Grimaldi, D. & Engels, M. S. (2005) Evolution of the Insects. New York: Cambridge University Press, pp. 755.Google Scholar
Hamilton, W. D. (1964) The genetical evolution of social behavior. II. Journal of Theoretical Biology 7, 1–52.CrossRefGoogle Scholar
Hamilton, W. D. (1972) Altruism and related phenomena, mainly in social insects. Annual Review of Ecology and Evolution, 3, 193–232.CrossRefGoogle Scholar
Hamilton, W. D. (1996) Narrow Roads of Gene Land, Vol. 1. Oxford: Oxford University Press.Google Scholar
Hattori, M. & Itino, T. (2008) Soldiers’ armature changes seasonally and locally in an eusocial aphid (Homoptera: Aphididae). Sociobiology, 52, 429–436.Google Scholar
Hattori, M., Kishida, O., & Itino, T. (2012) Buying time for colony mates: The anti-predatory function of soldiers in the eusocial aphid Ceratovacuna japonica (Homoptera, Hormaphidinae). Insectes Sociaux, 60, 15–21.CrossRefGoogle Scholar
Ijichi, N., Shibao, H., Miura, T., Matsumoto, T., & Fukatsu, T. (2005) Analysis of natural colonies of a social aphid Colophina arma: Population dynamics, reproductive schedule, and survey for ecological correlates with soldier production. Applied Entomology and Zoology, 40, 239–245.CrossRefGoogle Scholar
Inbar, M. (1998) Competition, territoriality & maternal defense in a gall-forming aphid. Ethology Ecology and Evolution, 10, 159–170.CrossRefGoogle Scholar
Inbar, M., Eshel, A., & Wool, D. (1995) Interspecific competition among phloem-feeding insects mediated by induced host-plant sinks. Ecology, 76, 1506–1515.CrossRefGoogle Scholar
Jaquiery, J., Stoeckel, S., Rispe, C., Mieuzet, L., Legeai, F., & Simon, J. C. (2012) Accelerated evolution of sex chromosomes in aphids, an X0 system. Molecular Biology and Evolution, 29, 837–847.CrossRefGoogle ScholarPubMed
Jedličková, V., Jedlička, P., & Lee, H.-J. (2015) Characterization and expression analysis of adipokinetic hormone and its receptor in eusocial aphid Pseudoregma bambucicola. General and Comparative Endocrinology, 223, 1–9.CrossRefGoogle ScholarPubMed
Kiester, A. R., & Strates, E. (1984) Social behavior in a thrips from Panama. Journal of Natural History, 18, 303–314.CrossRefGoogle Scholar
Kranz, B. D. (2005) Egg size and reproductive allocation in eusocial thrips. Behavioral Ecology, 16, 779–787.CrossRefGoogle Scholar
Kranz, B. D., Schwarz, M. P., Mound, L. A., & Crespi, B. J. (1999) Social biology and sex ratios of the eusocial gall-inducing thrips Kladothrips hamiltoni. Ecological Entomology, 24, 432–442.CrossRefGoogle Scholar
Kranz, B. D., Schwarz, M. P., Giles, L. C., & Crespi, B. J. (2000) Split sex ratios and virginity in a gall-inducing thrips. Journal of Evolutionary Biology, 13, 700–706.CrossRefGoogle Scholar
Kranz, B. D., Schwarz, M. P., Mound, L. A., & Crespi, B. J. (2001a) Social biology and sex ratios of the eusocial gall-inducing thrips Kladothrips hamiltoni. Ecological Entomology, 24, 432–442.CrossRefGoogle Scholar
Kranz, B. D., Chapman, T. W., Crespi, B. J., & Schwarz, M. P. (2001b) Social biology and sex ratios in the gall-inducing thrips, Oncothrips waterhousei and Oncothrips habrus. Insectes Sociaux, 48, 315–323.CrossRefGoogle Scholar
Kranz, B. D., Schwarz, M. P., Wills, T., Chapman, T. W., Morris, D. C., & Crespi, B. J. (2001c) A fully reproductive fighting morph in a soldier clade of gall-inducing thrips (Oncothrips morrisi). Behavioral Ecology and Sociobiology, 50, 151–161.CrossRefGoogle Scholar
Kranz, B. D., Schwarz, M. P., Morris, D. C., & Crespi, B. J. (2002) Life history of Kladothrips ellobus and Oncothrips rodwayi: Insight into the origin and loss of soldiers in gall-inducing thrips. Ecological Entomology, 27, 49–57.CrossRefGoogle Scholar
Kurosu, U. & Aoki, S. (2009) Extremely long-closed galls of a social aphid. Psyche: A Journal of Entomology, 2009, 1–9.CrossRefGoogle Scholar
Kurosu, U., Buranapanichpan, S., & Aoki, S. (2006) Astegopteryx spinocephala (Hemiptera: Aphididae), a new aphid species producing sterile soldiers that guard eggs laid in their gall. Entomological Science, 9, 181–190.CrossRefGoogle Scholar
Kutsukake, M., Shibao, H., Nikoh, N., et al. (2004) Venomous protease of aphid soldier for colony defense. Proceedings of the National Academy of Sciences of the United States of America, 101, 11338–11343.CrossRefGoogle ScholarPubMed
Kutsukake, M., Shibao, H., Uematsu, K., & Fukatsu, T. (2009) Scab formation and wound healing of plant tissue by soldier aphid. Proceedings of the Royal Society of London. Series B: Biological Sciences, 276, 1555–1563.Google ScholarPubMed
Lamb, R. J., MacKay, P. A., & Migui, S. M. (2012) Measuring the performance of aphids: Fecundity versus biomass. The Canadian Entomologist, 141, 401–405.CrossRefGoogle Scholar
Lawson, S. P., Legan, A. W., Graham, C., & Abbot, P. (2014a) Comparative phenotyping across a social transition in aphids. Animal Behaviour, 96, 117–125.CrossRefGoogle Scholar
Lawson, S. P., Christian, N., and Abbot, P. (2014b) Comparative analysis of the biodiversity of fungal endophytes in insect-induced galls and surrounding foliar tissue. Fungal Diversity, 66, 89–97.CrossRefGoogle Scholar
Lewis, T. (1973) Thrips, Their Biology, Ecology and Economic Importance. New York: Academic Press.Google Scholar
McLeish, M. J., Perry, S. P., Gruber, D., & Chapman, T. W. (2003) Dispersal patterns of an Australian gall-forming thrips and its host tree (Oncothrips tepperi and Acacia oswaldii). Ecological Entomology, 28, 243–246.CrossRefGoogle Scholar
McLeish, M. J., Chapman, T. W., & Crespi, B. J. (2006) Inbreeding ancestors: The role of sibmating in the social evolution of gall thrips. Journal of Heredity, 97, 31–38.CrossRefGoogle ScholarPubMed
McLeish, M. J., Crespi, B. J., Chapman, T. W., & Schwarz, M. P. (2007) Parallel diversification of Australian gall-thrips on Acacia. Molecular Phylogenetics and Evolution, 43, 714–725.CrossRefGoogle ScholarPubMed
Michener, C. D. (1969) Comparative social behavior of bees. Annual Review Of Entomology, 14, 299–342.CrossRefGoogle Scholar
Miller, D. G. III (1998) Consequences of communal gall occupation and a test for kin discrimination in the aphid Tamalia coweni (Cockerell) (Homoptera: Aphididae). Behavioral Ecology and Sociobiology, 43, 95–103.CrossRefGoogle Scholar
Miller, D. G. III (2005) Ecology and radiation of galling aphids (Tamalia; Hemiptera: Aphididae) on their host plants (Ericaceae). Basic and Applied Ecology, 6, 463–469.CrossRefGoogle Scholar
Miller, N. J., Kift, N. B., & Tatchell, G. M. (2005) Host-associated populations in the lettuce root aphid, Pemphigus bursarius (L.). Heredity, 94, 556–564.CrossRefGoogle ScholarPubMed
Minaei, K. (2014) New record of predatory thrips, Aeolothrips melaleucus (Thysanoptera, Aeolothripidae). Linzer Biologische Beitraege, 46, 637–642.Google Scholar
Moran, N. A. (1992) The evolution of aphid life cycles. Annual Review of Entomology, 37, 321–348.CrossRefGoogle Scholar
Moran, N. A. (1993a) Defenders in the North American aphid Pemphigus obesinymphae. Insectes Sociaux, 40, 391–402.CrossRefGoogle Scholar
Moran, N. A. (1993b) Evolution of sex ratio variation in aphids. In: Wrensch, D. L. & Ebbert, M. A. (eds.) Evolution and Diversity of Sex Ratio in Insects and Mites. New York: Chapman and Hall, pp. 346–368.CrossRefGoogle Scholar
Morris, D. C. & Schwarz, M. P. (2002) Pleometrosis in phyllode-glueing thrips (Thysanoptera: Phlaeothripidae) on Australian Acacia. Biological Journal of the Linnean Society, 75, 467–474.CrossRefGoogle Scholar
Morris, D. C., Schwarz, M. P., Crespi, B. J., & Cooper, S. J. B. (2001) Phylogenetics of gall-inducing thrips on Australian Acacia. Biological Journal of the Linnean Society, 74, 73–86.CrossRefGoogle Scholar
Morris, D. C., Schwarz, M. P., Cooper, S. J. B., & Mound, L. A. (2002) Phylogenetics of Australian Acacia thrips: The evolution of behavior and ecology. Molecular Phylogenetics and Evolution, 25, 278–292.CrossRefGoogle ScholarPubMed
Mound, L. A. (2005) Thysanoptera: Diversity and interactions. Annual Review of Entomology, 50, 247–269.CrossRefGoogle ScholarPubMed
Mound, L. A. & Morris, D. C. (2007) The insect order Thysanoptera: Classification versus systematics. Zootaxa, 1668, 395–411.CrossRefGoogle Scholar
Perry, S. P., McLeish, M. J., Schwarz, M. P., & Boyette, A. H. (2003) Variation in propensity to defend by reproductive gall morphs in two species of gall-forming thrips. Insectes Sociaux, 50, 54–58.CrossRefGoogle Scholar
Perry, S. P., Chapman, T. W., Schwarz, M. P., & Crespi, B. J. (2004) Proclivity and effectiveness in gall defense by soldiers in five species of gall-inducing thrips: Benefits of morphological caste dimorphism in two species (Kladothrips intermedius and K. habrus). Behavioral Ecology and Sociobiology, 56, 602–610.CrossRefGoogle Scholar
Pike, N. & Foster, W. A. (2008) The ecology of altruism in a clonal insect. In: Korb, J. & Heinze, J. (eds.) Ecology of Social Evolution. Berlin: Springer-Verlag, pp. 37–56.CrossRefGoogle Scholar
Pike, N., Richard, D., Foster, W., & Mahadevan, L. (2002) How aphids lose their marbles. Proceedings of the Royal Society of London. Series B: Biological Sciences, 269, 1211–1215.CrossRefGoogle ScholarPubMed
Pike, N., Braendle, C., & Foster, W. A. (2004) Seasonal extension of the soldier instar as a route to increased defense investment in the social aphid Pemphigus spyrothecae. Ecological Entomology, 29, 89–95.CrossRefGoogle Scholar
Pike, N., Whitfield, J.A., & Foster, W. A. (2007) Ecological correlates of sociality in Pemphigus aphids, with a partial phylogeny of the genus. BMC Evolutionary Biology, 7, 185.CrossRefGoogle ScholarPubMed
Pope, R. D. (1983) Some aphid waxes, their form and function (Homoptera: Aphididae). Journal of Natural History, 17, 489–506.CrossRefGoogle Scholar
Prokopy, R. J. & Roitberg, B. D. (2001) Joining and avoidance behavior in nonsocial insects. Annual Review Of Entomology, 46, 631–665.CrossRefGoogle ScholarPubMed
Queller, D. C. & Strassmann, J. E. (1998) Kin selection and social Insects. Bioscience, 48, 165–175.CrossRefGoogle Scholar
Rhoden, P. K. & Foster, W. A. (2002) Soldier behavior and division of labour in the aphid genus Pemphigus (Hemiptera, Aphididae). Insectes Sociaux, 49, 257–263.CrossRefGoogle Scholar
Roisen, Y. (2006) Life history, life types and caste evolution in termites. In: Kipyatkov, V. (ed.) Life Cycles in Social Insects: Behaviour, Ecology and Evolution. St. Petersburg: St. Petersburg University Press, pp. 85–95.Google Scholar
Rubenstein, D. R. & Lovette, I. J. (2007) Temporal environmental variability drives the evolution of cooperative breeding in birds. Current Biology, 17, 1414–1419.CrossRefGoogle ScholarPubMed
Schütze, M. & Maschwitz, U. (1991) Enemy recognition and defense within trophobiotic associations with ants by the soldier caste of Pseudoregma sundanica (Homoptera: Aphidoidea). Entomologia Generalis, 16, 1–12.CrossRefGoogle Scholar
Shibao, H. (1999) Lack of kin discrimination in the eusocial aphid Pseudoregma bambucicola (Homoptera: Aphididae). Journal of Ethology, 17, 17–24.CrossRefGoogle Scholar
Shibao, H., Lee, J.-M., Kutsukake, M., & Fukatsu, T. (2003) Aphid soldier differentiation: Density acts on both embryos and newborn nymphs. Naturwissenschaften, 90, 501–504.CrossRefGoogle ScholarPubMed
Shibao, H., Kutsukake, M., & Fukatsu, T. (2004a) The proximate cue of density-dependent soldier production in a social aphid. Journal of Insect Physiology, 50, 143–147.CrossRefGoogle Scholar
Shibao, H., Kutsukake, M., & Fukatsu, T. (2004b) Density triggers soldier production in a social aphid. Proceedings of the Royal Society of London. Series B: Biological Sciences, 271, Suppl, 3, S71–S74.CrossRefGoogle Scholar
Shibao, H., Kutsukake, M., Matsuyama, S., Fukatsu, T., & Shimada, M. (2010) Mechanisms regulating caste differentiation in an aphid social system. Communicative and Integrative Biology, 3, 1–5.CrossRefGoogle Scholar
Shingleton, A. W. & Foster, W. A. (2000) Ant tending influences soldier production in a social aphid. Proceedings of the Royal Society of London. Series B: Biological Sciences, 267, 1863–1868.CrossRefGoogle Scholar
Shingleton, A. W. & Foster, W. A. (2001) Behavior, morphology and the division of labour in two soldier-producing aphids. Animal Behaviour, 62, 671–679.CrossRefGoogle Scholar
Stern, D. L. (1994) A phylogenetic analysis of soldier evolution in the aphid family Hormaphididae. Proceedings of the Royal Society of London. Series B: Biological Sciences, 256, 203–209.Google ScholarPubMed
Stern, D. L. (1998) Phylogeny of the tribe Cerataphidini (Homoptera) and the evolution of the horned soldier aphids. Evolution, 52, 155.CrossRefGoogle ScholarPubMed
Stern, D. L. & Foster, W. A. (1996) The evolution of soldiers in aphids, Biological Reviews of the Cambridge Philosophical Society, 71, 27–79.CrossRefGoogle ScholarPubMed
Strassmann, J. E. & Queller, D. C. (2010) The social organism: Congresses, parties, and committees. Evolution, 64, 605–616.CrossRefGoogle ScholarPubMed
Stone, G. N. & Schönrogge, K. (2003) The adaptive significance of insect gall morphology. Trends in Ecology and Evolution, 18, 512–522.CrossRefGoogle Scholar
Toth, A. L., Varala, K., Newman, T. C., et al. (2007) Wasp gene expression supports an evolutionary link between maternal behavior and eusociality. Science, 318, 441–444.CrossRefGoogle ScholarPubMed
Turnbull, C., Hoggard, S., Gillings, M., et al. (2011) Antimicrobial strength increases with group size: Implications for social evolution. Biology Letters, 7, 249–252.CrossRefGoogle ScholarPubMed
Turnbull, C., Caravan, H., Chapman, T., et al. (2012) Antifungal activity in thrips soldiers suggests a dual role for this caste. Biology Letters, 8, 526–529.CrossRefGoogle ScholarPubMed
Wcislo, W. T. (1997) Are behavioral classifications blinders to studying natural variation? In: Choe, J. C. & Crespi, B. J. (eds.) The Evolution of Social Behavior in Insects and Arachnids. London: Cambridge University Press, pp. 8–13.CrossRefGoogle Scholar
Wcislo, W. T. & Tierney, S. M. (2009) The evolution of communal behavior in bees and wasps: An alternative to eusociality. In: Gadau, J. & Fewell, J. (eds.) Organization of Insect Societies. Cambridge: Harvard University Press, pp. 148–169.Google Scholar
Whitham, T. G. (1979) Territorial behavior of Pemphigus gall aphids. Nature, 279, 324–325.CrossRefGoogle Scholar
Whitham, T. G. (1986) Cost of benefits of territoriality: Behavioral and reproductive release by competing aphids. Ecology, 67, 139–147.CrossRefGoogle Scholar
Wilch, M. H. (1999) Predation and prey response in the galls of Pemphigus populi-ramulorum. Masters thesis, Tucson: University of Arizona.Google Scholar
Wills, T. E., Chapman, T. W., Kranz, B. D., & Schwarz, M. P. (2001) Reproductive division of labour coevolves with gall size in Australian thrips with soldiers. Naturwissenschaften, 88, 526–529.CrossRefGoogle ScholarPubMed
Wills, T. E., Chapman, T. W., & Mound, L. A. (2004) Natural history and description of Oncothrips kinchega, a new species of gall-inducing thrips with soldiers (Thysanoptera: Phlaeothripidae). Australian Journal of Entomology, 43, 169–176.CrossRefGoogle Scholar
Wilson, E. O. (1971) The Insect Societies. Cambridge: Harvard University Press.Google Scholar
Wilson, E. O. (1975) Sociobiology: The New Synthesis. Cambridge, MA: Harvard University Press, Belknap Press.Google Scholar
Withgott, J. H., Abbot, D. K., &. Moran, N. A (1997) Maternal death relaxes developmental inhibition in nymphal aphid defenders. Proceedings of the Royal Society B: Biological Sciences, 264, 1197–1202.CrossRefGoogle Scholar

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