Abstract
Solitary bees of the genus Tetrapedia have a specific association with mites of the genus Roubikia (Chaetodactylidae). These mites are frequently found attached to active Tetrapedia bees. We quantified the number of mites on individuals of Tetrapedia diversipes Klug and examined the interaction between these species. Nests of T. diversipes were obtained from trap-nests placed in four localities in São Paulo, Brazil. The study lasted from March 2007 to February 2009. Out of a total of 650 nests with emergences, 118 were infested with mites (Roubikia sp.). From these nests, 176 individuals of T. diversipes emerged with mites on their bodies. Additionally, six individuals of Coelioxoides waltheriae, the specific kleptoparasitic bee to T. diversipes, emerged. Mites were attached mainly to the mesosoma. All nests infected with mites did not presented mortality of the immature. The mortality rate of nests was inversely related to the level of mite infestation, suggesting a mutualistic interaction in which mites may remove fungi from the nests, while the bees would provide the mites with transport, dispersal, and shelter.
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References
Alves-dos-Santos I., Melo G.A.R., Rozen J.G. (2002) Biology and immature stages of the bee tribe Tetrapediini (Hymenoptera: Apidae), Am. Mus. Novitates 3377, 1–45.
Baker E.W., Roubik D.W., Delfinado-Baker M. (1987) The developmental stages and dimorphic males of Chaetodactylus panamensis, n. sp. (Acari: Chaetodactylidae) associated with solitary bee (Apoidea: Anthophoridae), Int. J. Acarol. 13, 65–73.
Biani N.B., Mueller U.G., Wcislo W.T. (2009) Cleaner mites: sanitary mutualism in the miniature ecosystem of neotropical bee bests, Am. Nat. 173, 841–847.
Camarotti-de-Lima M.F., Martins C.F. (2005) Biologia de nidificação e aspectos ecológicos de Anthodioctes lunatus (Smith) (Hymenoptera:Megachilidae, Anthidiini) em área de tabuleiro nordestino, PB. Neotrop. Entomol. 34, 375–380.
Camillo E. (2005) Nesting biology of four Tetrapedia species in trap-nests (Hymenoptera, Apidae, Tetrapediini), Rev. Biol. Trop. 53, 175–186.
Camillo E., Garófalo C.A., Serrano J.C., Mucilo G. (1995) Diversidade e abundância sazonal de abelhas e vespas solitárias em ninhos-armadilhas (Hymenoptera, Apocrita, Aculeata), Rev. Bras. Entomol. 39, 459–470.
Eickwort G.C. (1994) Evolution and life-history patterns of mites associated with bees, in: Houck MA (Ed.), Mites: Ecological and Evolutionary Analyses of Life-History Patterns, New York, Chapman & Hall, pp. 218–251.
Engel M.S. (2001) A monograph of the Baltic amber bees and evolution of the Apoidea (Hymenoptera), Bull. Am. Mus. Nat. Hist. 259, 1–192.
Fain A. (1966) Notes sur la biologie des acariens du genre Chaetodactylus et en particulier de C. osmiae, parasite des abeilles solitaires Osmia rufa et O. cornuta en Belgique (Sarcoptiformes: Chaetodactylidae), Bull. Ann. Soc. R. Belge Entomol. 102, 249–261.
Fain A. (1981) Notes on the hypopi of the genus Chaetodactylus Rondani, 1866 (Acari, Chaetodactylidae), Bull. Inst. R. Sci. Nat. Belg. Entomol. 53, 1–9.
Flechtmann C.H.W., Camargo C.A. (1974) Acari associated with stingless bees (Meliponidae, Hymenoptera) from Brazil, in: Piffl E. (Ed.), Proc. 4th Int. Congr. Acarol. Budapest, Académiai Kiadó, pp. 315–319.
Garófalo C.A., Martins C.F., Alves-dos-Santos I. (2004) The Brazilian solitary bee species caught in trap nests, in: International Workshop on solitary bees and their role in pollination, Beberibe, CE. Solitary Bees: conservation, rearing and management for pollination, Fortaleza: Impresa Universitária, pp. 77–84.
Houck M.A., O’Connor B.M. (1991) Ecological and evolutionary significance of phoresy in the Astigmata, Annu. Rev. Entomol. 36, 611–636.
Klimov P.B., O’Connor B.M. (2007) Ancestral area analysis of chaetodactylid mites (Acari: Chaetodactylidae), with description of new early derivative genus and six new species from the Neotropics, Ann. Entomol. Soc. Am. 100, 810–829.
Klimov P.B., O’Connor B.M. (2008) Morphology, Evolution, and Host Associations of Bee-Associated Mites of the Family Chaetodactylidae (Acari: Astigmata), with a monographic revision of North American taxa, Miscellaneous Publications, Museum of Zoology, University of Michigan 199, pp. 1–243.
Klimov P.B., O’Connor B.M., Knowles L.L. (2007a) Museum specimens and phylogenies elucidate ecology’s role in coevolutionary associations between mites and their bee hosts, Evolution 61, 1368–1379.
Klimov P.B., Vinson S.B., O’Connor B.M. (2007b) Acarinaria in associations of apid bees (Hymenoptera) and chaetodactylid mites (Acari), Invertebr. Syst. 21, 109–136.
Krombein K.V. (1962) Natural history of Plummers Island, Maryland. XVI. Biological notes on Chaetodactylus krombeini Baker, a parasitic mite of the megachilid bee, Osmia (Osmia) lignaria Say (Acarina, Chaetodactylidae), Proc. Biol. Soc. Wash. 75, 237–250.
Menezes C., Coletto-Silva A., Gazeta G.S., Kerr W.E. (2009) Infestation by Pyemotes tritici (Acari, Pyemotidae) causes death of stingless bee colonies (Hymenoptera: Meliponina), Genet. Mol. Res. 8, 630–634.
Michener C.D. (2000) The Bees of the World. Baltimore, The John Hopkins University Press.
Morato E.F. (2001) Biologia e ecologia de Anthodioctes morato Urban (Hymenoptera, Megachilidae, Anthidiini) em matas contínuas e fragmentos na Amazônia Central, Brasil. Rev. Bras. Zool. 18, 729–736.
O’Connor B.M. (1979) Evolutionary origins of astigmatid mites inhabiting stored products, in: Rodriguez J.G. (Ed.), Recent advances in acarology (1), Academic Press, New York, pp. 273–278.
O’Connor B.M. (1993a) The mite community associated with Xylocopa latipes (Hymenoptera: Anthophoridae: Xylocopinae) with description of a new type of acarinarium, Int. J. Acarol. 19, 159–166.
O’Connor B.M. (1993b) Generic relationships in the Chaetodactylidae (Acari: Astigmata) with description of a new genus, Acarologia 34, 345–362.
O’Connor B.M., Klompen J.S.H. (1999) Phylogenetic perspectives on mite-insect associations: the evolution of acarinaria, in: Needham G.R., Mitchell R., Horn D.J., Welbourn W.C. (Eds.), Acarology IX, Vol. 2, Symposia. Columbus, Ohio, Ohio Biological Survey, pp. 63–71.
Okabe K., Makino S. (2002) Phoretic mite fauna on the large carpenter bee Xylocopa appendiculata circumvolans (Hymenoptera: Apidae) with descriptions of its acarinaria on both sexes, J. Acarol. Soc. Jpn 11, 73–84.
Oldroyd B.P. (1999) Coevolution while you wait: Varroa jacobsoni, a new parasite of western honeybees, Trends. Ecol. Evol. 14, 312–315.
Park Y.L., Kondo V., White J., West T., McConnell B., McCutcheon T. (2009) Nest-to-nest dispersal of Chaetodactylus krombeini (Acari, Chaetodactylidae) associated with Osmia cornifrons (Hym., Megachilidae), J. Appl. Entomol. 133, 174–180.
Qu D., Maeta Y., Goubara M., Nakatsuka K.J., Kozo J., Kenji K. (2002) Reproductive strategy in the two species of cleptoparasitic astigmatid mites, Chaetodactylus nipponicus and Tortonia sp. (Acari: Chaetodactylidae and Suidasiidae), infesting Osmia cornifrons (Hymenoptera: Megachilidae). I. Invasion/infestation patterns and partial use of the host food, Jpn J. Entomol. 5, 121–141.
Roubik D.W. (1987) Notes on the biology of anthophorid bee Tetrapedia and the mite Chaetodactylus panamensis Baker, Roubik and Delfinado-Baker (Acari: Chaetodactylidae), Int. J. Acarol. 13, 75–76.
Schwarz H.H., Huck K. (1997) Phoretic mites use flowers to transfer between foraging bumblebees, Insectes Soc. 44, 303–310.
Trouessart E.L. (1904) Sur la coexistence de deux formes d’Hypopes dans une même espèce, chez la Acariens du genre Trichotarsus,. C. R. Soc. Biol. 56, 234–237.
Vicidomini S. (1996) Biologia di Xylocopa (Xylocopa) violacea (L., 1758) (Hymenoptera: Apidae): interazione con Sennertia (Sennertia) cerambycina (Acari Chaetodactylidae), Boll. Zool. Agr. Bachic. 28, 71–76.
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Cordeiro, G.D., Taniguchi, M., Flechtmann, C.H.W. et al. Phoretic mites (Acari: Chaetodactylidae) associated with the solitary bee Tetrapedia diversipes (Apidae: Tetrapediini). Apidologie 42, 128–139 (2011). https://doi.org/10.1051/apido/2010044
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DOI: https://doi.org/10.1051/apido/2010044