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Journal of Pest Science

, Volume 92, Issue 1, pp 327–341 | Cite as

Vertical and horizontal distribution of bark and woodboring beetles by feeding guild: is there an optimal trap location for detection?

  • Thomas N. SheehanEmail author
  • Michael D. Ulyshen
  • Scott Horn
  • E. Richard Hoebeke
Original Paper
  • 167 Downloads

Abstract

Bark and woodboring beetles include some of the most economically important forest pests. Understanding how these species are distributed in forests is critical for optimizing detection strategies. We placed traps at three heights above ground level at the edge and in the interior of two forests and focused on two groups: phloem/wood-feeding beetles (Coleoptera: Buprestidae, Cerambycidae, and some Curculionidae: Scolytinae) and ambrosia beetles (Coleoptera: Curculionidae: Scolytinae and Platypodinae). We recorded temperature, humidity, and canopy cover for each trap. Species richness increased with height for phloem-/wood-feeding beetles and decreased with height for ambrosia beetles, even when microclimatic variables were included in the models. Community composition differed greatly among heights but little between horizontal placements. Indicator species analysis found eight species (seven of which were phloem/wood feeders) to be significantly associated with traps at 15 m and eight species (six of which were ambrosia beetles) associated with traps at 0 m. Only one species was significantly associated with the forest edge and one species associated with the interior, but a total of thirteen species were associated with particular combinations of horizontal placement and height. While distance from the forest edge was an important factor for some species, trap height more strongly influenced the species of phloem-/wood-feeding and ambrosia beetles captured and is a more important consideration with respect to optimizing trapping programs.

Keywords

Bark and ambrosia beetles Saproxylic Microclimate Non-native species Invasive 

Notes

Acknowledgements

We thank Mike Hunter and Mike Wharton for permission to conduct this study at Whitehall and Tallassee Forests, respectively. We are also grateful to Carl Jordan and Chris Canalos for facilitating access to Tallassee Forest. We thank Conor Fair, Tommy McElrath, and Brad Hounkpati for assistance with fieldwork and Courtney Brissey who helped with species identification and field work. We are grateful to Joe McHugh for access to resources from his laboratory. We thank Dan Miller and Chris Crowe for access to a reference collection and advice on the project, as well as Mengyao Li, Xianyan Chen, and Funing Chen for statistical consultation. We also thank Jeremy Allison for advice on trap design and three anonymous reviewers for comments that greatly improved the manuscript. This study was funded by the USDA Forest Service Southern Research Station.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Human and animal rights

This article does not contain any studies with human participants or animals performed by any of the authors. The use of product names does not imply endorsement by the United States Department of Agriculture, the University of Georgia, or the Joseph W. Jones Ecological Research Center.

Supplementary material

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Supplementary material 1 (DOCX 12 kb)
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Supplementary material 3 (DOCX 14 kb)
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Supplementary material 4 (DOCX 14 kb)

References

  1. Aavik T, Ülle J, Liira J, Tulva I, Zobel M (2008) Plant diversity in a calcareous wooded meadow – The significance of management continuity. J Veg Sci 19(4):475–484.  https://doi.org/10.3170/2008-8-18380 Google Scholar
  2. Allison JD, Redak RA (2017) The impact of trap type and design features on survey and detection of bark and woodboring beetles and their associates: a review and meta-analysis. Annu Rev Entomol 62:127–146.  https://doi.org/10.1146/annurev-ento-010715-023516 Google Scholar
  3. Allison JD, Johnson CW, Meeker JR, Strom BL, Butler SM (2011) Effect of aerosol surface lubricants on the abundance and richness of selected forest insects captured in multiple-funnel and panel traps. J Econ Entomol 104(4):1258–1264.  https://doi.org/10.1603/EC11044 Google Scholar
  4. Allison JD, Bhandari BD, McKenney JL, Millar JG (2014) Design factors that influence the performance of flight intercept traps for the capture of longhorned beetles (Coleoptera: Cerambycidae) from the subfamilies Lamiinae and Cerambycinae. PLoS ONE 9(3):e93203.  https://doi.org/10.1371/journal.pone.0093203 Google Scholar
  5. Anderson RS (2002) Curculionidae Latreille 1802. In: Arnett RH Jr, Thomas MC, Skelley PE, Frank JH (eds) American beetles, volume II: Polyphaga: Scarabaeoidea through Curculionoidea. CRC Press, Boca Raton, pp 722–815Google Scholar
  6. Atkinson TH, Foltz JL, Connor MD (1988) Flight patterns of phloem- and wood-boring Coleoptera (Scolytidae, Platypodidae, Curculionidae, Buprestidae, Cerambycidae) in a north Florida slash pine plantation. Environ Entomol 17(2):259–265.  https://doi.org/10.1093/ee/17.2.259 Google Scholar
  7. Barringer L (2016) First record of the camphor shot borer, Cnestus mutilatus (Blandford) (Coleoptera: Curculionidae: Scolytinae) in Pennsylvania. Insecta Mundi 519:1–2Google Scholar
  8. Basset Y, Hammond PM, Barrios H, Holloway JD, Miller SE (2003) Vertical stratification of arthropod assemblages. In: Basset Y, Novotny V, Miller SE, Kitching RL (eds) Arthropods of tropical forests: spatio-temporal dynamics and resource use in the canopy. Cambridge University Press, Cambridge, pp 17–27Google Scholar
  9. Beaver RA (1986) The taxonomy, mycangia and biology of Hypothenemus curtipennis (Schedl), the first known cryphaline ambrosia beetle (Coleoptera: Scolytidae). Ent Scand 17(1):131–135Google Scholar
  10. Bellamy CL, Nelson GH (2002) Buprestidae Leach 1815. In: Arnett RH Jr, Thomas MC, Skelley PE, Frank JH (eds) American beetles, volume II: Polyphaga: Scarabaeoidea through Curculionoidea. CRC Press, Boca Raton, pp 98–112Google Scholar
  11. Bellard C, Cassey P, Blackburn TM (2016) Alien species as a driver of recent extinctions. Biol Lett 12:20150623.  https://doi.org/10.1098/rsbl.2015.0623 Google Scholar
  12. Berkov A (2018) Seasonality and stratification: Neotropical saproxylic beetles respond to a heat and moisture continuum with conservatism and plasticity. In: Ulyshen MD (ed) Saproxylic insects: diversity, ecology and conservation. Springer, Heidelberg, pp 547–578Google Scholar
  13. Beutenmuller W (1896) Food-habits of North American Cerambycidae. J NY Entomol Soc 4(2):73–81Google Scholar
  14. Bouget C, Brin A, Brustel H (2011) Exploring the “last biotic frontier”: are temperate forest canopies special for saproxylic beetles? For Ecol Manag 261:211–220.  https://doi.org/10.1016/j.foreco.2010.10.007 Google Scholar
  15. Brockerhoff EG, Jones DC, Kimberley MO, Suckling DM, Donaldson T (2006) Nationwide survey for invasive wood-boring and bark beetles (Coleoptera) using traps baited with pheromones and kairomones. For Ecol Manag 228:234–240.  https://doi.org/10.1016/j.foreco.2006.02.046 Google Scholar
  16. Buse J, Schröder B, Assmann T (2007) Modelling habitat and spatial distribution of an endangered longhorn beetle—a case study for saproxylic insect conservation. Biol Cons 137(3):372–381.  https://doi.org/10.1016/j.biocon.2007.02.025 Google Scholar
  17. Chen Y, Seybold SJ (2014) Crepuscular flight activity of an invasive insect governed by interacting abiotic factors. PLoS ONE 9(8):e105945.  https://doi.org/10.1371/journal.pone.0105945 Google Scholar
  18. Cognato AI, Hoebeke ER, Kajimura H, Smith SM (2015) History of the exotic ambrosia beetles Euwallacea interjectus and Euwallacea validus (Coleoptera: Curculionidae: Xyleborini) in the United States. J Econ Entomol 108(3):1129–1135.  https://doi.org/10.1093/jee/tov073 Google Scholar
  19. Colwell RK, Chao A, Gotelli NJ, Lin S, Mao CX, Chazdon RL, Longino JT (2012) Models and estimators linking individual-based and sample-based rarefaction, extrapolation and comparison of assemblages. J Plant Ecol 5(1):3–21.  https://doi.org/10.1093/jpe/rtr044 Google Scholar
  20. Davis AJ, Sutton SL, Brendell MJD (2011) Vertical distribution of beetles in a tropical rainforest in Sulawesi: the role of the canopy in contributing to biodiversity. Sepilok Bull 13(14):59–83Google Scholar
  21. de Groot P, Nott RW (2003) Response of Monochamus (Col. Cerambycidae) and some Buprestidae to flight intercept traps. J Appl Entomol 127(9–10):548–552.  https://doi.org/10.1046/j.1439-0418.2003.00799.x Google Scholar
  22. Didham RP, Ewers RM (2014) Edge effects disrupt vertical stratification of microclimate in a temperate forest canopy. Pac Sci 68(4):493–508.  https://doi.org/10.2984/68.4.4 Google Scholar
  23. Dodds KJ (2014) Effects of trap height on captures of arboreal insects in pine stands of northeastern United States of America. Can Entomol 146:80–89.  https://doi.org/10.4039/tce.2013.57 Google Scholar
  24. Dodds KJ, Dubois GD, Hoebeke ER (2010) Trap type, lure placement, and habitat effects on Cerambycidae and Scolytinae (Coleoptera) catches in northeastern United States. J Econ Entomol 103(3):698–707.  https://doi.org/10.1603/EC09395 Google Scholar
  25. Dodds KJ, Allison JD, Miller DR, Hanavan RP, Sweeney J (2015) Considering species richness and rarity when selecting optimal survey traps: comparisons of semiochemical baited flight intercept traps for Cerambycidae in eastern North America. Agric For Entomol 17(1):36–47.  https://doi.org/10.1111/afe.12078 Google Scholar
  26. Drury DW, Whitesell ME, Wade MJ (2016) The effects of temperature, relative humidity, light, and resource quality on flight initiation in the red flour beetle, Tribolium castaneum. Entomol Exp Appl 158(3):269–274.  https://doi.org/10.1111/eea.12401 Google Scholar
  27. Dufrêne M, Legendre P (1997) Species assemblages and indicator species: The need for a flexible asymmetrical approach. Ecol Monograph 67(3): 345–366. https://doi.org/10.1890/0012-9615(1997)067[0345:saaist]2.0.co;2Google Scholar
  28. Fraedrich SW, Harrington TC, Rabaglia RJ, Ulyshen MD, Mayfield AE, Hanula JL, Eickwort JM, Miller DR (2008) A fungal symbiont of the redbay ambrosia beetle causes a lethal wilt in redbay and other Lauraceae in the southeastern United States. Plant Dis 92(2):215–224.  https://doi.org/10.1094/PDIS-92-2-0215 Google Scholar
  29. Francese JA, Oliver JB, Fraser I, Lance DR, Youssef N, Sawyer AJ, Mastro VC (2008) Influence of trap placement and design on capture of the emerald ash borer (Coleoptera: Buprestidae). J Econ Entomol 101(6):1831–1837.  https://doi.org/10.1603/0022-0493-101.6.1831 Google Scholar
  30. Gandhi KJK, Audley J, Johnson J, Raines M (2009) Camphor shot borer, Xylosandrus mutilatus (Blandford) (Coleoptera: Curculionidae), an adventive ambrosia beetle in Georgia. Coleopt Bull 63(4):497–500Google Scholar
  31. Gossner MM (2009) Light intensity affects spatial distribution of Heteroptera in deciduous forests. Eur J Entomol 106(2):241–252.  https://doi.org/10.14411/eje.2009.032 Google Scholar
  32. Gotelli NJ, Colwell RK (2001) Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness. Ecol Lett 4:379–391.  https://doi.org/10.1046/j.1461-0248.2001.00230.x Google Scholar
  33. Graham EE, Mitchell RF, Reagel PF, Barbour JD, Millar JG, Hanks LM (2010) Treating panel traps with a fluoropolymer enhances their efficiency in capturing Cerambycid beetles. J Econ Entomol 103(3):641–647.  https://doi.org/10.1603/EC10013 Google Scholar
  34. Graham EE, Poland TM, McCullough DG, Millar JG (2012) A comparison of trap type and height for capturing cerambycid beetles (Coleoptera). J Econ Entomol 105(3):837–846.  https://doi.org/10.1603/EC12053 Google Scholar
  35. Grimbacher PS, Stork NE (2007) Vertical stratification of feeding guilds and body size in beetle assemblages from an Australian tropical rainforest. Austral Ecol 32(1):77–85.  https://doi.org/10.1111/j.1442-9993.2007.01735.x Google Scholar
  36. Hajek AE, St. Leger RJ (1994) Interactions between fungal pathogens and insect hosts. Annu Rev Entomol 39:293–322.  https://doi.org/10.1146/annurev.en.39.010194.001453 Google Scholar
  37. Hanks LM, Paine TD, Millar JG, Campbell CD, Schuch UK (1999) Water relations of host trees and resistance to the phloem-boring beetle Phoracantha semipunctata F. (Coleoptera: Cerambycidae). Oecologia 119(3):400–407.  https://doi.org/10.1007/s004420050801 Google Scholar
  38. Harpootlian PJ, Bellamy CL (2014) Jewel beetles (Coleoptera: Buprestidae) of South Carolina. South Carolina Agriculture Forest Research System, ClemsonGoogle Scholar
  39. Heepe L, Wolff JO, Gorb SN (2016) Influence of ambient humidity on the attachment ability of ladybird beetles (Coccinella septempunctata). Beilstein J Nanotech 7:1322–1329.  https://doi.org/10.3762/bjnano.7.123 Google Scholar
  40. Herms A, McCullough DG (2014) Emerald ash borer invasion of North America: history, biology, ecology, impacts, and management. Annu Rev Entomol 59:13–30.  https://doi.org/10.1146/annurev-ento-011613-162051 Google Scholar
  41. Holdsworth S, Hammond PM, Eggleton P (2016) Assessing high compositional differences of beetle assemblages across vertical woodland strata in the New Forest, Hampshire, England. J Nat Hist 50(39–40):2477–2485.  https://doi.org/10.1080/00222933.2016.1195022 Google Scholar
  42. Hulcr J, Stelinski LL (2017) The ambrosia symbiosis: from evolutionary ecology to practical management. Ann Rev Entomol 62:285–303.  https://doi.org/10.1146/annurev-ento-031616-035105 Google Scholar
  43. Jaworski T, Hilszczański J (2013) The effect of temperature and humidity changes on insects development their impact on forest ecosystems in the expected climate change. For Res Pap 74(4):345–355.  https://doi.org/10.2478/frp-2013-0033 Google Scholar
  44. Jonsell M, Weslien J, Ehnström B (1998) Substrate requirements of red-listed saproxylic invertebrates in Sweden. Biodivers Conserv 7(6):749–764.  https://doi.org/10.1023/A:1008888319031 Google Scholar
  45. Kajimura H, Hijii N (1992) Dynamics of the fungal symbionts in the gallery system and the mycangia of the ambrosia beetle, Xylosandrus mutilatus (Blandford) (Coleoptera: Scolytidae) in relation to its life history. Ecol Res 7:107–117.  https://doi.org/10.1007/BF02348489 Google Scholar
  46. King JR, Warren RJ, Bradford MA (2013) Social insects dominate eastern U.S. temperate hardwood forest macroinvertebrate communities in warmer regions. PLoS ONE 8(10):e75843.  https://doi.org/10.1371/journal.pone.0075843 Google Scholar
  47. Kirkendall LR, Biedermann PHW, Jordal BH (2015) Evolution and diversity of bark and ambrosia beetles. In: Vega FE, Hofstetter RW (eds) Bark beetles: biology and ecology of native and invasive species. Elsevier, New York, pp 85–156Google Scholar
  48. Leavengood JM (2013) First record of the camphor shot borer, Cnestus mutilatus (Blandford) (Curculionidae: Scolytinae: Xyleborini) in Kentucky. Insecta Mundi 308:1–3Google Scholar
  49. Leksono AS, Takada K, Koji S, Nakagoshi N, Anggraeni T, Nakamura K (2005) Vertical and seasonal distribution of flying beetles in a suburban temperate deciduous forest collected by water pan trap. Insect Sci 12(3):199–206.  https://doi.org/10.1111/j.1744-7917.2005.00025.x Google Scholar
  50. Lindhe A, Lindelöw A, Åsenblad N (2005) Saproxylic beetles in standing dead wood density in relation to substrate sun-exposure and diameter. Biodivers Conserv 14(12):3033–3053.  https://doi.org/10.1007/s10531-004-0314-y Google Scholar
  51. Lingafelter SW (2007) Illustrated key to the longhorned woodboring beetles of the Eastern United States. Coleopterists Society, North PotomacGoogle Scholar
  52. Maguire DY, Robert K, Brochu K, Larrivée M, Buddle CM, Wheeler TA (2014) Vertical stratification of beetles (Coleoptera) and flies (Diptera) in temperate forest canopies. Environ Entomol 43(1):9–17.  https://doi.org/10.1603/EN13056 Google Scholar
  53. McCune B, Mefford MJ (2011) PC-ORD. Multivariate analysis of ecological data. Version 6. MjM Software, Gleneden Beach, Oregon, USAGoogle Scholar
  54. Mendel Z, Boneh O, Shenhar Y, Riov J (1991) Diurnal flight patterns of Orthotomicus erosus and Pityogenes calcaratus in Israel. Phytoparasitica 19(1):23–31.  https://doi.org/10.1007/BF02981008 Google Scholar
  55. Miller DR, Duerr DA (2008) Comparison of arboreal beetle catches in wet and dry collection cups with Lindgren multiple funnel traps. J Econ Entomol 101(1):107–13. https://doi.org/10.1603/0022-0493(2008)101[107:coabci]2.0.co;2Google Scholar
  56. Miller DR, Crowe CM, Barnes BF, Gandhi KJ, Duerr DA (2013) Attaching lures to multiple-funnel traps targeting saproxylic beetles (Coleoptera) in pine stands: inside or outside funnels? J Econ Entomol 106(1):206–214.  https://doi.org/10.1603/EC12254 Google Scholar
  57. Miller DR, Crowe CM, Dodds KJ, Galligan LD, de Grott P, Hoebeke ER, Mayfield AE, Poland TM, Raffa KF, Sweeney JD (2015) Ipsenol, ipsdienol, ethanol, and α-pinene: trap lure blend for Cerambycidae and Buprestidae (Coleoptera) in pine forests of eastern North America. J Econ Entomol 108(4):1837–1851.  https://doi.org/10.1093/jee/tov126 Google Scholar
  58. Mooney HA, Cleland EE (2001) The evolutionary impact of invasive species. Proc Natl Acad Sci USA 98(10):5446–5451.  https://doi.org/10.1073/pnas.091093398 Google Scholar
  59. Morewood WD, Hein KE, Katinic PJ, Borden JH (2002) An improved trap for large wood-boring insects, with special reference to Monochamus scutellatus (Coleoptera: Cerambycidae). Can J Forest Res 32(3):519–525.  https://doi.org/10.1139/x01-224 Google Scholar
  60. Nowak DJ, Pasek JE, Sequeira RA, Crane DE, Mastro VC (2001) Potential effect of Anoplophora glabripennis (Coleoptera: Cerambycidae) on urban trees in the United States. J Econ Entomol 94(1):116–122.  https://doi.org/10.1603/0022-0493-94.1.116 Google Scholar
  61. Nowakowski AJ, Maerz JC (2009) Estimation of larval stream salamander densities in three proximate streams in the Georgia Piedmont. J Herpetol 43(3):503–509.  https://doi.org/10.1670/07-128R2.1 Google Scholar
  62. Östrand F, Anderbrant O (2003) From where are insects recruited? A new model to interpret catches of attractive traps. Agric For Entomol 5(2):163–171.  https://doi.org/10.1046/j.1461-9563.2003.00174.x Google Scholar
  63. Pawson SM, Marcot BG, Woodberry OG (2017) Predicting forest insect flight activity: a bayesian network approach. PLoS ONE 12(9):e0183464.  https://doi.org/10.1371/journal.pone.0183464 Google Scholar
  64. Pimentel D, Zuniga R, Morrison D (2005) Update on the environmental and economic costs associated with alien-invasive species in the United States. Ecol Econ 52(3):273–288.  https://doi.org/10.1016/j.ecolecon.2004.10.002 Google Scholar
  65. Porter K (2014) Tallassee Forest Athens-Clarke County, Georgia: inventories, baseline data and recommendations by contributors. Oconee Rivers Greenway Commission, AthensGoogle Scholar
  66. Procházka J, Cizek L, Schlaghamerský J (2018) Vertical stratification of scolytine beetles in temperate forests. Insect Conserv Divers.  https://doi.org/10.1111/icad.12301 Google Scholar
  67. Rabaglia R, Dole SA, Cognato AI (2006) Review of American Xyleborina (Coleoptera: Curculionidae: Scolytinae) occurring north of Mexico, with an illustrated key. Ann Entomol Soc Am 99(6): 1034-1056. https://doi.org/10.1603/0013-8746(2006)99[1034:roaxcc]2.0.co;2Google Scholar
  68. Rabaglia R, Duerr D, Acciavatti R, Ragenovich I (2008) Early detection and rapid response for non-native bark and ambrosia beetles. US Deparment Agric-Forest Service, Forest Health Protection, WashingtonGoogle Scholar
  69. Rassati D, Marini L, Marchioro M, Rapuzzi P, Magnani G, Poloni R, Di Giovanni F, Mayo P, Sweeney J (2018) Developing trapping protocols for wood-boring beetles associated with broadleaf trees. J Pest Sci.  https://doi.org/10.1007/s10340-018-0984-y Google Scholar
  70. SAS Institute (1999) SAS system for windows, version 8 Cary, NCGoogle Scholar
  71. Schiefer TL, Bright DE (2004) Xylosandrus mutilatus (Blandford), an exotic ambrosia beetle (Coleoptera: Curculionidae: Scolytinae: Xyleborini) new to North America. Coleopts Bull 58(3):431–438.  https://doi.org/10.1649/760 Google Scholar
  72. Schmeelk TC, Millar JG, Hanks LM (2016) Species diversity of Cerambycid beetles captured in forests of east-central Illinois. J Econ Entomol 109(4):1750–1757.  https://doi.org/10.1093/jee/tow102 Google Scholar
  73. Sebek P, Vodka S, Bogusch P, Pech P, Tropek R, Weiss M, Zimova K, Cizek L (2016) Open-grown trees as key habitats for arthropods in temperate woodlands: the diversity, composition, and conservation value of associated communities. For Ecol Manag 380:172–181.  https://doi.org/10.1016/j.foreco.2016.08.052 Google Scholar
  74. Spiegel KS, Leege LM (2013) Impacts of laurel wilt disease on redbay (Persea borbonia (L.) Spreng.) population structure and forest communities in the coastal plain of Georgia, USA. Biol Invasions 15(11):2467–2487.  https://doi.org/10.1007/s10530-013-0467-2 Google Scholar
  75. Stireman JO, Cerretti P, Whitmore D, Hardersen S, Gianelle D (2012) Composition and stratification of a tachinid (Diptera: Tachinidae) parasitoid community in a European temperate plain forest. Insect Conserv Diver 5(5):346–357.  https://doi.org/10.1111/j.1752-4598.2011.00168.x Google Scholar
  76. Stone WD, Nebeker TE, Gerard PD (2007) Host plants of Xylosandrus mutilatus in Mississippi. Fla Entomologist 90(1):191-195. https://doi.org/10.1653/0015-4040(2007)90[191:hpoxmi]2.0.co;2Google Scholar
  77. Stork NE, Stone M, Sam L (2016) Vertical stratification of beetles in tropical rainforests as sampled by light traps in North Queensland, Australia. Austral Ecol 41(2):168–178.  https://doi.org/10.1111/aec.12286 Google Scholar
  78. Turnbow RH, Thomas MC (2002) Cerambycidae Leach 1805. In: Arnett RH Jr, Thomas MC, Skelley PE, Frank JH (eds) American beetles, volume II: Polyphaga: Scarabaeoidea through Curculionoidea. CRC Press, Boca Raton, pp 568–601Google Scholar
  79. Ulyshen MD (2011) Arthropod vertical stratification in temperate deciduous forests: implications for conservation-oriented management. For Ecol Manag 261(9):1479–1489.  https://doi.org/10.1016/j.foreco.2011.01.033 Google Scholar
  80. Ulyshen MD, Hanula JL (2007) A comparison of the beetle (Coleoptera) fauna captured at two heights above the ground in a North American temperate deciduous forest. Am Midl Nat 158(2):260–78. https://doi.org/10.1674/0003-0031(2007)158[260:acotbc]2.0.co;2Google Scholar
  81. Ulyshen MD, Sheehan TN (2017) Trap height considerations for detecting two economically important forest beetle guilds in southeastern US forests. J Pest Sci.  https://doi.org/10.1007/s10340-017-0883-7 Google Scholar
  82. Vance CC, Kirby KR, Malcolm JR, Smith SM (2003) Community composition of longhorned beetles (Coleoptera: Cerambycidae) in the canopy and understory of sugar maple and white pine stands in south-central Ohio. Environ Entomol 32(5):1066–1074.  https://doi.org/10.1603/0046-225X-32.5.1066 Google Scholar
  83. Vega FE, Infante F, Johnson AJ (2015) The genus Hypothenemus, with emphasis on H. hampei, the coffee berry borer. In: Vega FE, Hofstetter RW (eds) Bark beetles: biology and ecology of native and invasive species. Elsevier, New York, pp 427–494Google Scholar
  84. Vodka Š, Cizek L (2013) The effects of edge-interior and understorey-canopy gradients on the distribution of saproxylic beetles in a temperate lowland forest. For Ecol Manag 304:33–41.  https://doi.org/10.1016/j.foreco.2013.04.007 Google Scholar
  85. Vodka Š, Konvicka M, Cizek L (2009) Habitat preferences of oak-feeding xylophagous beetles in a temperate woodland: implications for forest history and management. J Insect Conserv 13(5):553.  https://doi.org/10.1007/s10841-008-9202-1 Google Scholar
  86. Walsh JR, Carpenter SR, Vander Zanden MJ (2016) Invasive species triggers a massive loss of ecosystem services through a trophic cascade. P Natl Acad Sci USA 113(15):4081–4085.  https://doi.org/10.1073/pnas.1600366113 Google Scholar
  87. Wan FH, Yang NW (2016) Invasion and management of agricultural alien insects in China. Annu Rev Entomol 61:77–98.  https://doi.org/10.1146/annurev-ento-010715-023916 Google Scholar
  88. Webster RP, Alderson CA, Webster VL, Hughes CC, Sweeney JD (2016) Further contributions to the longhorn beetle (Coleoptera, Cerambycidae) fauna of New Brunswick and Nova Scotia, Canada. ZooKeys 552:109–122.  https://doi.org/10.3897/zookeys.552.6039 Google Scholar
  89. Weiss M, Procházka J, Schlaghamerský J, Cizek L (2016) Fine-Scale vertical stratification and guild composition of saproxylic beetles in lowland and montane forests: similar patterns despite low faunal overlap. PLoS ONE 11(3):e0149506.  https://doi.org/10.1371/journal.pone.0149506 Google Scholar
  90. Werle CT, Sampson BJ, Oliver JB (2011) Diversity, abundance, and seasonality of ambrosia beetles (Coleoptera: Curculionidae) in southern Mississippi. Midsouth Entomol 5:1–5Google Scholar
  91. Wermelinger B, Flückiger PF, Obrist MK, Duelli P (2007) Horizontal and vertical distribution of saproxylic beetles (Col., Buprestidae, Cerambycidae, Scolytinae) across sections of forest edges. J Appl Entomol 131(2):104–114.  https://doi.org/10.1111/j.1439-0418.2006.01128.x Google Scholar
  92. Wilcove DS, Rothstein D, Dubow J, Phillips A, Losos E (1998) Quantifying threats to imperiled species in the United States. Bioscience 48(8):607–615.  https://doi.org/10.2307/1313420 Google Scholar
  93. Wood SL (1982) The bark and ambrosia beetles of North and Central America (Coleoptera: Scolytidae), a taxonomic monograph. Great Basin Nat Mem Num 6:1359Google Scholar
  94. Wylie FR, Griffiths M, King J (2008) Development of hazard site surveillance programs for forest invasive species: a case study from Brisbane, Australia. Aust For 71(3):229–235.  https://doi.org/10.1080/00049158.2008.10675040 Google Scholar
  95. Zhang Y, Limin W, Kongming W, Wyckhuys KAG, Heimpel GE (2008) Flight performance of the soybean aphid, Aphis glycines (Hemiptera: Aphididae) under different temperature and humidity regimens. Environ Entomol 37(2):301–306.  https://doi.org/10.1093/ee/37.2.301 Google Scholar

Copyright information

© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2018

Authors and Affiliations

  • Thomas N. Sheehan
    • 1
    • 2
    Email author
  • Michael D. Ulyshen
    • 3
  • Scott Horn
    • 3
  • E. Richard Hoebeke
    • 4
  1. 1.Department of EntomologyUniversity of GeorgiaAthensUSA
  2. 2.Joseph W. Jones Ecological Research Center at IchauwayNewtonUSA
  3. 3.USDA Forest Service, Southern Research StationAthensUSA
  4. 4.Museum of Natural History and Department of EntomologyUniversity of GeorgiaAthensUSA

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