Artificial covering on trap nests improves the colonization of trap-nesting wasps

To evaluate the role that a trap-nest cover might have on sampling methodologies, the abundance of each species of trap-nesting Hymenoptera and the parasitism rate in a Canadian forest were compared between artificially covered and uncovered traps. Of trap tubes exposed at eight forest sites in six...

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Published inJournal of applied entomology (1986) Vol. 132; no. 3; pp. 225 - 229
Main Authors Taki, Hisatomo, Kevan, Peter G, Viana, Blandina F, Silva, Fabiana O, Buck, Matthias
Format Journal Article
LanguageEnglish
Published Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.04.2008
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Abstract To evaluate the role that a trap-nest cover might have on sampling methodologies, the abundance of each species of trap-nesting Hymenoptera and the parasitism rate in a Canadian forest were compared between artificially covered and uncovered traps. Of trap tubes exposed at eight forest sites in six trap-nest boxes, 531 trap tubes were occupied and 1216 individuals of 12 wasp species of four predatory families, Vespidae (Eumeninae), Crabronidae, Sphecidae and Pompilidae emerged over 2 years, and no bee species were found. Results indicated that artificial covering led to a significant increase in the number of nested tubes of Ancistrocerus adiabatus, Ancistrocerus antilope, Ancistrocerus campestris and Auplopus mellipes, and significant effects of covering were not found for the other species. No significant difference in the overall parasitism rate between covered and uncovered traps was noted. These suggested that the covering technique could provide more opportunities for some wasp species to colonize trap nests.
AbstractList To evaluate the role that a trap-nest cover might have on sampling methodologies, the abundance of each species of trap-nesting Hymenoptera and the parasitism rate in a Canadian forest were compared between artificially covered and uncovered traps. Of trap tubes exposed at eight forest sites in six trap-nest boxes, 531 trap tubes were occupied and 1216 individuals of 12 wasp species of four predatory families, Vespidae (Eumeninae), Crabronidae, Sphecidae and Pompilidae emerged over 2 years, and no bee species were found. Results indicated that artificial covering led to a significant increase in the number of nested tubes of Ancistrocerus adiabatus, Ancistrocerus antilope, Ancistrocerus campestris and Auplopus mellipes, and significant effects of covering were not found for the other species. No significant difference in the overall parasitism rate between covered and uncovered traps was noted. These suggested that the covering technique could provide more opportunities for some wasp species to colonize trap nests.
To evaluate the role that a trap‐nest cover might have on sampling methodologies, the abundance of each species of trap‐nesting Hymenoptera and the parasitism rate in a Canadian forest were compared between artificially covered and uncovered traps. Of trap tubes exposed at eight forest sites in six trap‐nest boxes, 531 trap tubes were occupied and 1216 individuals of 12 wasp species of four predatory families, Vespidae (Eumeninae), Crabronidae, Sphecidae and Pompilidae emerged over 2 years, and no bee species were found. Results indicated that artificial covering led to a significant increase in the number of nested tubes of Ancistrocerus adiabatus , Ancistrocerus antilope , Ancistrocerus campestris and Auplopus mellipes , and significant effects of covering were not found for the other species. No significant difference in the overall parasitism rate between covered and uncovered traps was noted. These suggested that the covering technique could provide more opportunities for some wasp species to colonize trap nests.
Author Kevan, Peter G.
Taki, Hisatomo
Viana, Blandina F.
Buck, Matthias
Silva, Fabiana O.
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Issue 3
Keywords Nesting
Forests
bee
Carolinian forest
aculeate
Insecta
trap-nesting wasps
Trap
cavity nesting
Arthropoda
Parasitism rate
Hymenoptera
Invertebrata
Nest
Colonization
Aculeata
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References_xml – reference: Klein AM, Steffan-Dewenter I, Tscharntke T, 2006. Rain forest promotes trophic interactions and diversity of trap-nesting hymenoptera in adjacent agroforestry. J. Anim. Ecol. 75, 315-323.
– reference: Allen GM, Eagles PFJ, Price SD, 1990. Conserving Carolinian Canada. University of Waterloo Press, Waterloo.
– reference: Gaston KJ, Smith RM, Thompson K, Warren PH, 2005. Urban domestic gardens (II): Experimental tests of methods for increasing biodiversity. Biodivers. Conserv. 14, 395-413.
– reference: Krombein KV, 1967. Trap-nesting wasps and bees: life histories, nests and associates. Smithsonian Institution Press, Washington DC.
– reference: Tylianakis JM, Klein AM, Lozada T, Tscharntke T, 2006a. Spatial scale of observation affects alpha, beta and gamma diversity of cavity-nesting bees and wasps across a tropical land-use gradient. J. Biogeogr. 33, 1295-1304.
– reference: Frankie GW, Vinson SB, Newman LE, Barthell JF, 1988. Nest site and habitat preference of Centris bees in the Costa Rican dry forest. Biotropica 20, 301-310.
– reference: Steffan-Dewenter I, 2002. Landscape context affects trap-nesting bees, wasps, and their natural enemies. Ecol. Entomol. 27, 631-637.
– reference: Argus GW, 1992. The phytogeography of rare vascular plants in Ontario and its bearing on plant conservation. Can. J. Bot. 70, 469-490.
– reference: Collins JA, Jennings DT, 1987. Spruce budworm and other lepidopterous prey of eumedid wasps Hymenoptera Eumenidae in spruce-fir forests of Main USA. Great Lakes Entomol. 20, 127-134.
– reference: Tylianakis JM, Klein AM, Tscharntke T, 2005. Spatiotemporal variation in the diversity of hymenoptera across a tropical habitat gradient. Ecology 86, 3296-3302.
– reference: Klein AM, Steffan-Dewenter I, Tscharntke T, 2003. Pollination of Coffea canephora in relation to local and regional agroforestry management. J. Appl. Ecol. 40, 837-845.
– reference: Jennings DT, Houseweart MW, 1984. Predation by eumenid wasps Hymenoptera Eumenidae on spruce budworm Choristoneura fumiferana Lepidoptera Tortricidae and other lepidopterous larvae in spruce fir forest of Main. Ann. Entomol. Soc. Am. 77, 39-45.
– reference: Tylianakis JM, Tscharntke T, Lewis OT, 2007. Habitat modification alters the structure of tropical host-parasitoid food webs. Nature 445, 202-205.
– reference: Wearing CH, Harris AC, 2005. Evaluation of the predatory wasp, Ancistrocerus gazella, for biological control of leafrollers in Otago fruit crops. II. Wasp phenology and seasonal changes in prey composition. Biocontrol Sci. Techn. 15, 281-298.
– reference: Taki H, Boone JW, Viana BF, Silva FO, Kevan PG, Sheffield CS, 2004. Effect of shading on trap nest utilization by hole-nesting aculeate Hymenoptera. Can. Entomol. 136, 889-891.
– reference: Tylianakis JM, Tscharntke T, Klein AM, 2006b. Diversity, ecosystem function, and stability of parasitoid host interactions across a tropical habitat gradient. Ecology 87, 3047-3057.
– reference: Crawley MJ, 2005. Statistics: an introduction using R. John Wiley, New York.
– reference: Godfrey S, Hilton DFJ, 1983. Nesting biology of solitary wasps and bees in the eastern townships region, Quebec. Can. Field Nat. 97, 1-8.
– reference: Harris AC, 1994. Ancistrocerus gazella (Hymenoptera: Vespoidea: Eumenidae): a potentially useful biological control agent for leafrollers Plantortix octo, P. excessana, Ctenopseustis obliqua, C. herana, and Epiphyas postvittana (Lepidoptera: Tortricidae) in New Zealand. New Zeal. J. Crop Hort. 22, 235-238.
– reference: Waldron G, 2003. Trees of the Carolinian forest: a guide to species, their ecology and uses. Boston Mills Press, Toronto.
– reference: Bohart RM, Kimsey LS, 1982. A synopsis of the Chrysididae in America north of Mexico. Mem. Am. Entomol. Inst. 33, 1-266.
– reference: R Development Core Team, 2006. R: a language and environment for statistical computing. R foundation for statistical computing, Vienna.
– reference: Tscharntke T, Gathmann A, Steffan-Dwenter I, 1998. Bioindication using trap-nesting wasps and their natural enemies: community structure and interactions. J. Appl. Ecol. 35, 708-719.
– reference: Griswold T, 2001. Two new species of trap-nesting Anthidiini (Hymenoptera: Megachilidae) from Sri Lanka. Proc. Entomol. Soc. Wash. 103, 269-273.
– reference: Taki H, Viana BF, Kevan PG, Silva FO, Buck M, 2008. Does forest loss affect the communities of trap-nesting wasps (Hymenoptera: Aculeata) in forests? Landscape vs. local habitat conditions. J. of Insect Conserv. 12, 15-21.
– reference: Faraway JJ, 2006. Extending the linear model with R. Chapman and Hall, Boca Raton, FL.
– reference: Wearing CH, Harris AC, 1999. Evaluation of the predatory wasp, Ancistrocerus gazella, for biological control of leafrollers in Otago fruit crops: I. Prey composition, nest structure and wasp productivity from artificial nests. Biocontrol Sci. Technol. 9, 315-325.
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Snippet To evaluate the role that a trap-nest cover might have on sampling methodologies, the abundance of each species of trap-nesting Hymenoptera and the parasitism...
To evaluate the role that a trap‐nest cover might have on sampling methodologies, the abundance of each species of trap‐nesting Hymenoptera and the parasitism...
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StartPage 225
SubjectTerms aculeate
Ancistrocerus antilope
Animal and plant ecology
Animal, plant and microbial ecology
Apoidea
bee
Biological and medical sciences
Carolinian forest
cavity nesting
Crabronidae
forests
Fundamental and applied biological sciences. Psychology
nests
parasitism
Pompilidae
Sphecidae
Synecology
Terrestrial ecosystems
trap-nesting wasps
traps
Title Artificial covering on trap nests improves the colonization of trap-nesting wasps
URI https://api.istex.fr/ark:/67375/WNG-4SBLF9LT-R/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1439-0418.2007.01237.x
https://www.proquest.com/docview/47583553
Volume 132
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