Register      Login
Invertebrate Systematics Invertebrate Systematics Society
Systematics, phylogeny and biogeography
RESEARCH ARTICLE

Systematics of new subsocial and solitary Australasian Anelosimus species (Araneae : Theridiidae)

Ingi Agnarsson
+ Author Affiliations
- Author Affiliations

A University of Puerto Rico, Rio Piedras, San Juan, PR, 00931, Puerto Rico, USA.

B Department of Entomology, National Museum of Natural History, Smithsonian Institution, NHB-105, PO Box 37012, Washington, DC 20013-7012, USA.

C Email: iagnarsson@gmail.com

Invertebrate Systematics 26(1) 1-16 https://doi.org/10.1071/IS11039
Submitted: 29 September 2011  Accepted: 2 December 2011   Published: 19 June 2012

Abstract

Species of the cobweb spider genus Anelosimus range from solitary to subsocial to social, and sociality has evolved repeatedly within the genus. Thus, this genus allows studies of the traits that play a role in social evolution. However, taxonomic knowledge of Anelosimus is geographically narrow and nearly all sociobiological studies have been done in the Americas. Only one behaviourally unknown species has been described from all of Australasia. Here, I describe seven new Anelosimus from Papua New Guinea (Anelosimus potmosbi, sp. nov., Anelosimus pomio, sp. nov., Anelosimus eidur, sp. nov. and Anelosimus luckyi, sp. nov.), Bali (Anelosimus bali, sp. nov.), Australia (Anelosimus pratchetti, sp. nov.) and an unknown locality (Anelosimus terraincognita, sp. nov.), ranging from solitary to subsocial. A phylogenetic analysis supports the inclusion of these species in Anelosimus, and suggests that solitary Papuan species represent a second reversal from subsocial behaviour. Both solitary species inhabit the beachfront, a habitat that appears not to be conducive to social behaviour in spiders. Subsocial species, as in other parts of the world, are found in montane tropical forests of Papua New Guinea, and at relatively high latitudes in Australia. Thus, a global ecological pattern of sociality in Anelosimus is emerging as taxonomic, phylogenetic and ethological knowledge extends beyond the Americas.

Additional keywords: Australia, Bali, evolution of sociality, New Britain, Papua New Guinea, social ecology, taxonomy.


References

Agnarsson, I. (2004). Morphological phylogeny of cobweb spiders and their relatives (Araneae, Araneoidea, Theridiidae). Zoological Journal of the Linnean Society 141, 447–626.
Morphological phylogeny of cobweb spiders and their relatives (Araneae, Araneoidea, Theridiidae).Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I. (2005). Revision and phylogenetic analysis of American ethicus and rupununi groups of Anelosimus (Araneae, Theridiidae). Zoologica Scripta 34, 389–413.
Revision and phylogenetic analysis of American ethicus and rupununi groups of Anelosimus (Araneae, Theridiidae).Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I. (2006). A revision of the New World eximius lineage of Anelosimus (Araneae, Theridiidae) and a phylogenetic analysis using worldwide exemplars. Zoological Journal of the Linnean Society 146, 453–593.
A revision of the New World eximius lineage of Anelosimus (Araneae, Theridiidae) and a phylogenetic analysis using worldwide exemplars.Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I. (2010). The utility of ITS2 in spider phylogenetics: notes on prior work and an example from Anelosimus. The Journal of Arachnology 38, 377–382.
The utility of ITS2 in spider phylogenetics: notes on prior work and an example from Anelosimus.Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I. (2012). A new phylogeny of Anelosimus and the placement and behavior of Anelosimus vierae n.sp. from Uruguay (Araneae: Theridiidae). The Journal of Arachnology 40, 78–84.
A new phylogeny of Anelosimus and the placement and behavior of Anelosimus vierae n.sp. from Uruguay (Araneae: Theridiidae).Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I., and Kuntner, M. (2005). Madagascar: an unexpected hotspot of social Anelosimus spider diversity (Araneae: Theridiidae). Systematic Entomology 30, 575–592.
Madagascar: an unexpected hotspot of social Anelosimus spider diversity (Araneae: Theridiidae).Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I., and Zhang, J. X. (2006). New species of Anelosimus (Araneae: Theridiidae) from Africa and Southeast Asia, with notes on sociality and color polymorphism. Zootaxa 1147, 1–34.

Agnarsson, I., Avilés, L., Coddington, J. A., and Maddison, W. P. (2006a). Sociality in theridiid spiders: repeated origins of an evolutionary dead end. Evolution 60, 2342–2351.

Agnarsson, I., Barrantes, G., and May-Collado, L. J. (2006b). Notes on the biology of Anelosimus pacificus Levi, 1963 (Theridiidae, Araneae) – evidence for an evolutionary reversal to a less social state. Journal of Natural History 40, 2681–2687.
Notes on the biology of Anelosimus pacificus Levi, 1963 (Theridiidae, Araneae) – evidence for an evolutionary reversal to a less social state.Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I., Maddison, W. P., and Avilés, L. (2007). The phylogeny of the social Anelosimus spiders (Araneae: Theridiidae) inferred from six molecular loci and morphology. Molecular Phylogenetics and Evolution 43, 833–851.
The phylogeny of the social Anelosimus spiders (Araneae: Theridiidae) inferred from six molecular loci and morphology.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXlvVOrurk%3D&md5=78a4dd256081f8741507616db9b45920CAS |

Agnarsson, I., Kuntner, M., Coddington, J. A., and Blackledge, T. A. (2010a). Shifting continents, not behaviours: independent colonization of solitary and subsocial Anelosimus spider lineages on Madagascar (Araneae, Theridiidae). Zoologica Scripta 39, 75–87.
Shifting continents, not behaviours: independent colonization of solitary and subsocial Anelosimus spider lineages on Madagascar (Araneae, Theridiidae).Crossref | GoogleScholarGoogle Scholar |

Agnarsson, I., Maddison, W. P., and Avilés, L. (2010b). Complete separation along matrilines in a social spider metapopulation inferred from hypervariable mitochondrial DNA region. Molecular Ecology 19, 3052–3063.
Complete separation along matrilines in a social spider metapopulation inferred from hypervariable mitochondrial DNA region.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtFCgtb3J&md5=f49f00b85364d596b2e02dd23330fd59CAS |

Avilés, L. (1997). Causes and consequences of cooperation and permanent-sociality in spiders. In ‘The Evolution of Social Behaviour in Insects and Arachnids’. (Eds J. C. Choe and B. J. Crespi.) pp. 476–498. (Cambridge University Press: Cambridge, UK.)

Avilés, L. (2000). Nomadic behaviour and colony fission in a cooperative spider: life history evolution at the level of the colony? Biological Journal of the Linnean Society. Linnean Society of London 70, 325–339.
Nomadic behaviour and colony fission in a cooperative spider: life history evolution at the level of the colony?Crossref | GoogleScholarGoogle Scholar |

Avilés, L., and Gelsey, G. (1998). Natal dispersal and demography of a subsocial Anelosimus species and its implications for the evolution of sociality in spiders. Canadian Journal of Zoology – Revue Canadienne De Zoologie 76, 2137–2147.

Avilés, L., and Purcell, J. (2011). Anelosimus oritoyacu, a cloud forest social spider with only slightly female-biased primary sex ratios. The Journal of Arachnology 39, 178–182.
Anelosimus oritoyacu, a cloud forest social spider with only slightly female-biased primary sex ratios.Crossref | GoogleScholarGoogle Scholar |

Avilés, L., Maddison, W. P., and Agnarsson, I. (2006). A new independently derived social spider with explosive colony proliferation and a female size dimorphism. Biotropica 38, 743–753.
A new independently derived social spider with explosive colony proliferation and a female size dimorphism.Crossref | GoogleScholarGoogle Scholar |

Avilés, L., Agnarsson, I., Salazar, P. A., Purcell, J., Iturralde, G., Yip, E. C., Powers, K. S., and Bukowski, T. C. (2007). Natural history miscellany – altitudinal patterns of spider sociality and the biology of a new midelevation social Anelosimus species in Ecuador. American Naturalist 170, 783–792.
Natural history miscellany – altitudinal patterns of spider sociality and the biology of a new midelevation social Anelosimus species in Ecuador.Crossref | GoogleScholarGoogle Scholar |

Bellemain, E., and Ricklefs, R. E. (2008). Are islands the end of the colonization road? Trends in Ecology & Evolution 23, 461–468.
Are islands the end of the colonization road?Crossref | GoogleScholarGoogle Scholar |

Bilde, T., Lubin, Y., Smith, D., Schneider, J. M., and Maklakov, A. A. (2005). The transition to social inbred mating systems in spiders: role of inbreeding tolerance in a subsocial predecessor. Evolution 59, 160–174.

Bilde, T., Coates, K. S., Birkhofer, K., Bird, T., Maklakov, A. A., Lubin, Y., and Avilés, L. (2007a). Survival benefits select for group living in a social spider despite reproductive costs. Journal of Evolutionary Biology 20, 2412–2426.
Survival benefits select for group living in a social spider despite reproductive costs.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2snjt1ersA%3D%3D&md5=952793de27fb2bc6875b44d665839aafCAS |

Bilde, T., Maklakov, A. A., and Schilling, N. (2007b). Inbreeding avoidance in spiders: evidence for rescue effect in fecundity of female spiders with outbreeding opportunity. Journal of Evolutionary Biology 20, 1237–1242.
Inbreeding avoidance in spiders: evidence for rescue effect in fecundity of female spiders with outbreeding opportunity.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2s3lvVarsA%3D%3D&md5=f530c1e15e6cbf314db94a16611f3b37CAS |

Bilde, T., Tuni, C., Cariani, A., Santini, A., Tabarroni, C., Garoia, F., and Goodacre, S. L. (2009). Characterization of microsatellite loci in the subsocial spider Stegodyphus lineatus (Araneae: Eresidae). Molecular Ecology Resources 9, 128–130.
Characterization of microsatellite loci in the subsocial spider Stegodyphus lineatus (Araneae: Eresidae).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXjtFGmsb4%3D&md5=3cb7d26ec07c6c3a8efcff0aa95e203bCAS |

Bukowski, T. C., and Avilés, L. (2002). Asynchronous maturation of the sexes may limit close inbreeding in a subsocial spider. Canadian Journal of Zoology – Revue Canadienne De Zoologie 80, 193–198.
Asynchronous maturation of the sexes may limit close inbreeding in a subsocial spider.Crossref | GoogleScholarGoogle Scholar |

Delbarco-Trillo, J., Burkert, B. A., Goodwin, T. E., and Drea, C. M. (2011). Night and day: the comparative study of strepsirrhine primates reveals socioecological and phylogenetic patterns in olfactory signals. Journal of Evolutionary Biology 24, 82–98.
Night and day: the comparative study of strepsirrhine primates reveals socioecological and phylogenetic patterns in olfactory signals.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXivVOltbs%3D&md5=4f73f3ef7bf52f301046d51a4823c29fCAS |

Fox, C. W., and Reed, D. H. (2010). Inbreeding depression increases with maternal age in a seed-feeding beetle. Evolutionary Ecology Research 12, 961–972.

Fox, C. W., Stillwell, R. C., Wallin, W. G., Curtis, C. L., and Reed, D. H. (2011). Inbreeding-environment interactions for fitness: complex relationships between inbreeding depression and temperature stress in a seed-feeding beetle. Evolutionary Ecology 25, 25–43.
Inbreeding-environment interactions for fitness: complex relationships between inbreeding depression and temperature stress in a seed-feeding beetle.Crossref | GoogleScholarGoogle Scholar |

Green, P. (1999). PHRAP, 0.990329 edn. Available at http://phrap.org/ [Verified January 2012]

Green, P., and Ewing, B. (2002). PHRED, 0.020425c edn. Available at http://phrap.org/ [Verified January 2012]

Guevara, J., and Avilés, L. (2007). Multiple techniques confirm elevational differences in insect size that may influence spider sociality. Ecology 88, 2015–2023.
Multiple techniques confirm elevational differences in insect size that may influence spider sociality.Crossref | GoogleScholarGoogle Scholar |

Guevara, J., and Avilés, L. (2009). Elevational changes in the composition of insects and other terrestrial arthropods at tropical latitudes: a comparison of multiple sampling methods and social spider diets. Insect Conservation and Diversity 2, 142–152.
Elevational changes in the composition of insects and other terrestrial arthropods at tropical latitudes: a comparison of multiple sampling methods and social spider diets.Crossref | GoogleScholarGoogle Scholar |

Guevara, J., Gonzaga, M. O., Vasconcellos-Neto, J., and Avilés, L. (2011). Sociality and resource use: insights from a community of social spiders in Brazil. Behavioral Ecology 22, 630–638.
Sociality and resource use: insights from a community of social spiders in Brazil.Crossref | GoogleScholarGoogle Scholar |

Heaney, L. R. (2007). Is a new paradigm emerging for oceanic island biogeography? Journal of Biogeography 34, 753–757.
Is a new paradigm emerging for oceanic island biogeography?Crossref | GoogleScholarGoogle Scholar |

Hirsch, B. T., and Maldonado, J. E. (2011). Familiarity breeds progeny: sociality increases reproductive success in adult male ring-tailed coatis (Nasua nasua). Molecular Ecology 20, 409–419.
Familiarity breeds progeny: sociality increases reproductive success in adult male ring-tailed coatis (Nasua nasua).Crossref | GoogleScholarGoogle Scholar |

Huelsenbeck, J. P., and Ronquist, R. (2001). MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17, 754–755.
MRBAYES: Bayesian inference of phylogenetic trees.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3MvotV2isw%3D%3D&md5=89aaec60163cef8dac4fe0ecf046c64cCAS |

Johannesen, J., Lubin, Y., Smith, D. R., Bilde, T., and Schneider, J. M. (2007). The age and evolution of sociality in Stegodyphus spiders: a molecular phylogenetic perspective. Proceedings of the Royal Society, Series B 274, 231–237.
The age and evolution of sociality in Stegodyphus spiders: a molecular phylogenetic perspective.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhsF2qsLc%3D&md5=d24bfad007fcd3f1fa3e832f0df58273CAS |

Johannesen, J., Moritz, R. F. A., Simunek, H., Seibt, U., and Wickler, W. (2009a). Species cohesion despite extreme inbreeding in a social spider. Journal of Evolutionary Biology 22, 1137–1142.
Species cohesion despite extreme inbreeding in a social spider.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3Mvgs1KltA%3D%3D&md5=f5b0224d6c64ab446fa1aa81ad9ef9d8CAS |

Johannesen, J., Wickler, W., Seibt, U., and Moritz, R. F. A. (2009b). Population history in social spiders repeated: colony structure and lineage evolution in Stegodyphus mimosarum (Eresidae). Molecular Ecology 18, 2812–2818.
Population history in social spiders repeated: colony structure and lineage evolution in Stegodyphus mimosarum (Eresidae).Crossref | GoogleScholarGoogle Scholar |

Lubin, Y., and Bilde, T. (2007). The evolution of sociality in spiders. Advances in the Study of Behavior 37, 83–145.
The evolution of sociality in spiders.Crossref | GoogleScholarGoogle Scholar |

Lubin, Y., Birkhofer, K., Berger-Tal, R., and Bilde, T. (2009). Limited male dispersal in a social spider with extreme inbreeding. Biological Journal of the Linnean Society. Linnean Society of London 97, 227–234.
Limited male dispersal in a social spider with extreme inbreeding.Crossref | GoogleScholarGoogle Scholar |

Maddison, D., and Maddison, W. (2011a). Chromaseq: a Mesquite module for analyzing sequence chromatograms. Version 0.99. Available at http://mesquiteproject.org/packages/chromaseq Verified January 2012]

Maddison, W., and Maddison, D. (2011b). Mesquite: a modular system for evolutionary analysis. Version 2.75. Available at http://mesquiteproject.org [Verified January 2012]

Okada, K., Blount, J. D., Sharma, M. D., Snook, R. R., and Hosken, D. J. (2011). Male attractiveness, fertility and susceptibility to oxidative stress are influenced by inbreeding in Drosophila simulans. Journal of Evolutionary Biology 24, 363–371.
Male attractiveness, fertility and susceptibility to oxidative stress are influenced by inbreeding in Drosophila simulans.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M7gslOgsw%3D%3D&md5=5bc3698e1369cc0a108b31392cbe81d8CAS |

Pagel, M. (1997). Inferring evolutionary processes from phylogenies. Zoologica Scripta 26, 331–348.
Inferring evolutionary processes from phylogenies.Crossref | GoogleScholarGoogle Scholar |

Posada, D. (2008). jModelTest: phylogenetic model averaging. Molecular Biology and Evolution 25, 1253–1256.
jModelTest: phylogenetic model averaging.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXotlKgsb4%3D&md5=8a1f07129ca906c4b292e237699ed9deCAS |

Purcell, J. (2011). Geographic patterns in the distribution of social systems in terrestrial arthropods. Biological Reviews of the Cambridge Philosophical Society 86, 475–491.
Geographic patterns in the distribution of social systems in terrestrial arthropods.Crossref | GoogleScholarGoogle Scholar |

Purcell, J., and Avilés, L. (2007). Smaller colonies and more solitary living mark higher elevation populations of a social spider. Journal of Animal Ecology 76, 590–597.
Smaller colonies and more solitary living mark higher elevation populations of a social spider.Crossref | GoogleScholarGoogle Scholar |

Purcell, J., and Avilés, L. (2008). Gradients of precipitation and ant abundance may contribute to the altitudinal range limit of subsocial spiders: insights from a transplant experiment. Proceedings of the Royal Society, Series B 275, 2617–2625.
Gradients of precipitation and ant abundance may contribute to the altitudinal range limit of subsocial spiders: insights from a transplant experiment.Crossref | GoogleScholarGoogle Scholar |

Roberts, M. J. (1989). Anelosimus pulchellus (Walckenaer, 1802): deletion from the list of British spider species. British Arachnological Society Newsletter 56, 3–4.

Ronquist, F., and Huelsenbeck, J. P. (2003). MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics (Oxford, England) 19, 1572–1574.
MrBayes 3: Bayesian phylogenetic inference under mixed models.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXntlKms7k%3D&md5=9c53a6e1009ac0a4829f70ecd07199e1CAS |

Rousselle, Y., Thomas, M., Galic, N., Bonnin, I., and Goldringer, I. (2011). Inbreeding depression and low between-population heterosis in recently diverged experimental populations of a selfing species. Heredity 106, 289–299.
Inbreeding depression and low between-population heterosis in recently diverged experimental populations of a selfing species.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M7itl2itg%3D%3D&md5=3a455ea76d5146857e5df153877d07fdCAS |

Ruch, J., Heinrich, L., Bilde, T., and Schneider, J. M. (2009a). The evolution of social inbreeding mating systems in spiders: limited male mating dispersal and lack of pre-copulatory inbreeding avoidance in a subsocial predecessor. Biological Journal of the Linnean Society. Linnean Society of London 98, 851–859.
The evolution of social inbreeding mating systems in spiders: limited male mating dispersal and lack of pre-copulatory inbreeding avoidance in a subsocial predecessor.Crossref | GoogleScholarGoogle Scholar |

Ruch, J., Heinrich, L., Bilde, T., and Schneider, J. M. (2009b). Relatedness facilitates cooperation in the subsocial spider, Stegodyphus tentoriicola. BMC Evolutionary Biology 9, 257.

Schneider, J. M., and Bilde, T. (2008). Benefits of cooperation with genetic kin in a subsocial spider. Proceedings of the National Academy of Sciences of the United States of America 105, 10843–10846.
Benefits of cooperation with genetic kin in a subsocial spider.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXpvFOju7k%3D&md5=400d872c1125958025f2bbb208c174cbCAS |

Simmons, L. W. (2011). Inbreeding depression in the competitive fertilization success of male crickets. Journal of Evolutionary Biology 24, 415–421.
Inbreeding depression in the competitive fertilization success of male crickets.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M7gslOgtQ%3D%3D&md5=33c37e167e35a755f96605da591a217cCAS |

Smith, D., van Rijn, S., Henschel, J., Bilde, T., and Lubin, Y. (2009). Amplified fragment length polymorphism fingerprints support limited gene flow among social spider populations. Biological Journal of the Linnean Society. Linnean Society of London 97, 235–246.
Amplified fragment length polymorphism fingerprints support limited gene flow among social spider populations.Crossref | GoogleScholarGoogle Scholar |

Thompson, J. D., Higgins, D. G., and Givson, T. J. (1994). CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalties and weight matrix choice. Nucleic Acids Research 22, 4673–4680.
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalties and weight matrix choice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXitlSgu74%3D&md5=30ced7c55989028a0f69fafe641cd83eCAS |

Vollrath, F. (1986). Environmental, reproduction and the sex ratio of the social spider Anelosimus eximius (Araneae, Theridiidae). The Journal of Arachnology 14, 267–281.

Yagi, N., and Hasegawa, E. (2011). Both cooperation and nest position improve larval survival in the sweat bee, Lasioglossum (Evylaeus) baleicum. Journal of Ethology 29, 63–67.
Both cooperation and nest position improve larval survival in the sweat bee, Lasioglossum (Evylaeus) baleicum.Crossref | GoogleScholarGoogle Scholar |

Yip, E. C., Powers, K. S., and Avilés, L. (2008). Cooperative capture of large prey solves scaling challenge faced by spider societies. Proceedings of the National Academy of Sciences of the United States of America 105, 11818–11822.
Cooperative capture of large prey solves scaling challenge faced by spider societies.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtVCnurrF&md5=a6c34f4597ceee9ea270639ddc71acfeCAS |

Zhang, B., Liu, L., and Zhang, F. (2011). The cobweb spiders of the genus Anelosimus Simon, 1891 (Araneae: Theridiidae) in Hainan Island, China. Zootaxa 2833, 49–59.