2005
DOI: 10.4039/n04-082
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Bark reflectance spectra of conifers and angiosperms: implications for host discrimination by coniferophagous bark and timber beetles

Abstract: The spectral reflectance of phytophagous insects' host plants is usually quantified between 300–350 nm (ultraviolet, UV) and 700 nm (farred to infrared), and the shape and magnitude of the distribution of reflected light determine the hue, saturation, and intensity perceived by insects (Moericke 1969). Host perception also depends on the distribution of environmental light (Endler 1993) and on the constraints of the insects' visual system, which is usually described as dichromatic, with one type of photorecept… Show more

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Cited by 30 publications
(40 citation statements)
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“…tree bark, for example, reßects uniformly little energy at all wavelengths except red, where it rises slightly (Prokopy and Owens 1983). A similar trend has been seen for measurements taken from several types of pine (Strom et al 1999, Campbell andBorden 2005) as well as varieties of black walnut, elm, hickory, and ash (D.W.B., unpublished results). Ongoing studies will examine the spectral properties of bark tissue from several ash species.…”
Section: Discussionsupporting
confidence: 66%
“…tree bark, for example, reßects uniformly little energy at all wavelengths except red, where it rises slightly (Prokopy and Owens 1983). A similar trend has been seen for measurements taken from several types of pine (Strom et al 1999, Campbell andBorden 2005) as well as varieties of black walnut, elm, hickory, and ash (D.W.B., unpublished results). Ongoing studies will examine the spectral properties of bark tissue from several ash species.…”
Section: Discussionsupporting
confidence: 66%
“…Processing time of collected beetles is reduced over earlier trap types, and the funnels collapse for easy storage and transport of the traps (Lindgren 1983). The Lindgren trap provides a dark, vertical silhouette with similar spectral reflectance properties to that of conifer tree hosts (Campbell and Borden 2005), which is an important component of host location for coniferophagous bark beetles (Campbell and Borden 2006). Attraction to aggregation pheromone-baited Lindgren funnel traps was reduced for three different species of bark beetles when the black funnels were replaced with white ones, suggesting that visual and olfactory cues are integrated in the host location process in bark beetles (Campbell and Borden 2006).…”
Section: Host Colonisation Semiochemicals For Monitoring and Control mentioning
confidence: 99%
“…Frisch (1966) was first to prove associative learning of colors in the honey bee, by showing how workers that had always been fed on blue paper could subsequently locate that color among various shades of grey. Campbell and Borden (2005) reported implications of the bark reflectance spectra of conifers and angiosperms for host discrimination by coniferophagous bark and timber beetles.…”
Section: Introductionmentioning
confidence: 97%