Evolution of coloration
Dr. Morehouse received his Ph.D. in 2009 with Ron Rutowski at Arizona State University, performed his postdoctoral studies with Jérôme Casas at the Université de Tours, France, and joined the Department in 2011
For nearly 15 years, Dr. Morehouse has been studying the traits that males and females use to interact, with a particular emphasis on color traits and the eyes that perceive them. Other recent interests include understanding co-evolutionary dynamics driving molecular interactions between male ejaculates and female reproductive tracts, nutritional ecology, and the evolution of organismal life histories. Prior to becoming an academic biologist, Dr. Morehouse was a salmon fisherman, a farmhand, a sommelier, and a musician.
As conspicuous members of every biological community, brightly colored animals have fascinated and puzzled us since time immemorial. They have also taught us much about the process of evolution, from Darwin’s early musings about sexual selection to contemporary work on hybrid speciation in mimetic butterflies. In the Morehouse lab, we seek fundamental insights into the evolution of bright coloration, focusing on how animals produce their colors, what they communicate with them, and how their visual systems perceive and process colorful signals. Our research draws from a broad range of techniques, integrating biophotonics, pigment biochemistry, animal behavior, visual ecology, developmental physiology, nutritional ecology and evolutionary genetics.
Animals use a bewildering array of mechanisms to produce color in their tissues, from pigments synthesized de novo to complex crystalline structures that selectively reflect certain wavelengths of light. Even in well studied animal groups, such as birds and fish, much remains unknown regarding how color is produced. We study the optical properties and basic constituents of colored animal tissues using electron and light microscopy, UV-vis microspectrophotometry, optical measurements, physical modeling, and biochemical techniques for pigment identification (see Fig. 1). Insects, spiders and birds are some of our favorite subjects, but we’re always open to looking at other systems.
Color signals are a key component of the umwelt of most higher animals. In fact, many animals have color vision that exceeds our own, with fine color discrimination extending into the UV and deep red. Our research seeks to enter this richer world of color to understand how and why animals use visual signals to communicate. We do this using behavioral assays, manipulations of visual signals, measurements of color patterns, light environments and visual system components, and mathematical modeling of the visual responses of focal species. We are interested in uncovering not only how specific animals communicate with color, but also broader themes in the co-evolution of visual signals and visual systems.
Color signals present unique opportunities to test fundamental evolutionary theory, from how ornaments exaggerate under directional female choice to resolutions of intralocus sexual conflict. Because they often require large quantities of limiting nutritional resources, color signals also compete with other key life history traits during development, making them important players in the evolution of life history strategies. Our research leverages techniques from nutritional ecology, developmental biology, experimental evolution and quantitative genetics to probe the evolutionary dynamics of color traits.
Feel free to email or call if you would like to know more about our research or how you can get involved.
Meslin, C., Plakke, M.S, Deutsch, A.B., Small, B.S., Morehouse, N.I., and Clark, N.L. 2015. Digestive organ in the female reproductive tract borrows genes from multiple organ systems to adopt critical functions. Molecular Biology and Evolution. In press.
Morehouse, N.I. 2014. Condition-dependent ornaments, life histories, and the evolving architecture of resource-use. Integrative and Comparative Biology, 54(4), 591-600. doi:10.1093/icv/icu103
Limeri, L.B. and Morehouse, N.I. 2014. Sensory biases and the maintenance of color polymorphisms: Viewing the Colias ‘alba’ polymorphism through the male visual system. Functional Ecology, 28(5), 1197-1207. doi: 10.1111/1365-2435.12244
Ligon, R.A., Dolezal, A.G., Hicks, M.R., Butler, M.W., Morehouse, N.I. and Ganesh, T.G. 2014. Using ants, animal behavior, and the learning cycle to investigate scientific processes. American Biology Teacher, 76, 52-534.
Taylor, L.A., Maier, E.B., Byrne, K.J., Amin, Z. and Morehouse, N.I. 2014. Colour use by tiny predators: Jumping spiders show colour biases during foraging. Animal Behaviour, 90, 149-157. doi: 10.1016/j.anbehav.2014.01.025
Hua, J., Morehouse, N.I. and Relyea, R. 2013. Pesticide resistance in amphibians: Induced resistance in susceptible populations, constitutive tolerance in tolerant populations. Evolutionary Applications, 6(7), 1028-1040. doi: 10.1111/eva.12083
Morehouse, N.I., Mandon, N., Christides, J.P., Body, M., Bimbard, G. and Casas, J. 2013. Seasonal selection and resource dynamics in a seasonally polyphenic butterfly. Journal of Evolutionary Biology, 26, 175-185. doi: 10.1111/jeb.12051
Meadows, M.G., Morehouse, N.I., Rutowski, R.L, Douglas, J.M. and McGraw, K.J. 2011. Quantifying iridescent coloration in animals: A method for improving repeatability. Behavioral Ecology and Sociobiology. 65(6), 1317-1327. doi: 10.1007/s00265-010-1135-5
Van Gossum, H., Bots, J, Van Heusden, J, Hammers, M., Katleen, H. and Morehouse, N.I. 2011. Reflectance spectra and morph mating frequencies support intraspecific mimicry in the female colour polymorphic damselfly Ischnura elegans. Evolutionary Ecology. 25(1), 139-154. doi: 10.1007/s10682-010-9388-z
Morehouse, N.I. and Rutowski, R.L. 2010. In the eyes of the beholders: Female choice and avian predation risk associated with an exaggerated male butterfly color. American Naturalist, 176(6), 768-784. doi:10.1086/657043
Morehouse, N.I., Nakazawa, T., Booher, C.M., Jeyasingh, P.D. and Hall, M.D. 2010. Sex in a material world: Why the study of sexual reproduction and sex-specific traits should become more nutritionally-explicit. Oikos, 119(5), 766-778. doi:10.1111/j.1600-0706.2009.18569.x
Morehouse, N.I. and Rutowski, R.L. 2010. Developmental responses to variable diet composition in the cabbage white butterfly, Pieris rapae: the role of nitrogen, carbohydrates and genotype. Oikos, 119(4), 636-645. doi:10.1111/j.1600-0706.2009.17866.x
Lindstedt, C., Morehouse, N.I., Pakkanen, H., Casas, J., Christides, J.P., Kemppainen, K., Lindström, L. and Mappes, J. 2010. Characterizing the pigment composition of a variable warning signal of Parasemia plantaginis larvae. Functional Ecology, 24(4): 759-766. doi: 10.1111/j.1365-2435.2010.01686.x
Morehouse, N.I. and Rutowski, R.L. 2009. Comment on “Floral iridescence, produced by diffraction optics, acts as a cue for animal pollinators.” Science, 325, 1072-d. doi:10.1126/science.1173324
Meadows, M.G., Butler, M.W., Morehouse, N.I., Taylor, L.A., Toomey, M.B., McGraw, K.J. and Rutowski, R.L. 2009. Iridescence: views from many angles. Journal of the Royal Society Interface, 6, S107-113. doi:10.1098/rsif.2009.0013.focus
Shawkey, M.D., Morehouse, N.I. and Vukusic, P. 2009. A protean palette: colour materials and mixing in birds and butterflies. Journal of the Royal Society Interface, 6, S221-S231. doi:10.1098/rsif.2008.0459.focus
Morehouse, N.I., Vukusic, P. and Rutowski, R.L. 2007. Pterin pigment granules are responsible for both broadband light scattering and wavelength selective absorption in the wing scales of pierid butterflies. Proceedings of the Royal Society of London B, 274, 359-366. doi:10.1098/rspb.2006.3730
McGraw, K.J., Toomey, M.B., Nolan, P.M., Morehouse, N.I., Massaro, M. and Jouventin, P. 2007. A description of unique fluorescent yellow pigments in penguin feathers. Pigment Cell Research, 20, 301-304. doi:10.1111/j.1600-0749.2007.00386.x
Rutowski, R.L., Macedonia, J., Merry, J., Morehouse, N.I., Yturralde, K., Taylor-Taft, L., Gaalema, D., Kemp, D.J. and Papke, R.S., 2007. Iridescent ultraviolet signaling in the Orange Sulphur butterfly (Colias eurytheme): Spatial, temporal and spectral properties. Biological Journal of the Linnean Society, 90, 349-364. doi:10.1111/j.1095-8312.2007.00749.x
Merry, J., Morehouse, N.I., Yturralde, K., and Rutowski, R.L., 2006. Eyes of a patrolling butterfly: Visual field and eye structure in the Orange Sulphur, Colias eurytheme (Lepidoptera, Pieridae). Journal of Insect Physiology, 52(3), 240-248. doi:10.1016/j.jinsphys.2005.11.002
Rutowski, R.L., Macedonia, J., Morehouse, N.I. and Taylor-Taft, L., 2005. Pterin pigments amplify iridescent ultraviolet signal in males of the orange sulphur butterfly, Colias eurytheme. Proceedings of the Royal Society of London B, 272, 2329-2335. doi:10.1098/rspb.2005.3216