By David B. Dusenbery (auth.), Professor Dr. Friedrich G. Barth, Professor Dr. Axel Schmid (eds.)
Sense organs function one of those organic interface among the surroundings and the organism. consequently, the connection among sensory platforms and ecology is especially shut and its wisdom of primary significance for an realizing of animal habit. The 16 chapters of this publication exemplify the variety of the limitations and possibilities linked to the feeling of stimuli representing diversified kinds of power. It stresses the occasions happening within the sensory outer edge the place the animal is uncovered to and will get in contact with its normal habitat and acquires the data had to manage its interplay with its environment.
Ecology of Sensing brings jointly the prime specialists within the field.
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Additional resources for Ecology of Sensing
Vision Res 36:1217-1224 Ichikawa T, Tateda H (1982) Distribution of color receptors in the larval eyes of four species of Lepidoptera. J Comp Physiol 149:317-324 Kitamoto J, Sakamoto K, Ozaki K, Mishina Y, Arikawa K (1998) Two visual pigments in a singe photoreceptor cell: identification and histological localization of three mRNAs encoding visual pigment opsins in the retina of the the butterfly Papilio xuthus. J Exp Biol201: 1255-1261 Lin SW, Kochendoerfer GG, Caroll KS, Wang D, Mathies RA, Sakmar TP (1998) Mechanisms of spectral tuning in blue cone pigments.
The problem is that we are not sure if these duplications are species specific, or whether they are more basal in larger taxonomic groups, such as genera or even orders. The butterflies Papilio glaucus and Papilio xuthus, for example, share two gene opsin gene duplications (Briscoe 1998a; Kitamoto et al. 1998); as do Drosophila melanogaster and Drosophila Why Sensory Ecology Needs to Become More Evolutionary 29 pseudoobscura (Zuker et al. 1985; Carulli and Hartl 1992). All other insects that have been surveyed for opsins have been undersampled, so that we cannot be sure how constrained individual species are in terms of photoreceptor number.
1993), the freshwaterdwelling bug Notonecta (Bmckmoser 1968), nocturnal hawkmoths (White et a!. 1994), and the larval ocelli of some Lepidoptera (Ichikawa and Tateda 1982) have similar sets of color receptors. On the basis of such difficulties, Goldsmith ( 1990) concluded that phylogenetic and molecular constraints might play more important a role in determining the wavelength positioning of color receptors than is good for any pan-adaptionist scenario. We wish to reiterate this warning, and to add several additional ones.