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Evolution
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Former Faculty

 

Dr. 
Tia-Lynn Ashman

Photo of Dr. 
Ashman

Plant Evolutionary Ecology
 
Associate Professor
 
Dr. Ashman received her Ph.D. in 1991 with M.L. Stanton at the University of California at Davis, performed her postdoctoral studies with DJ Schoen at McGill University, and joined the Department in 1994.

Currently, Dr. Ashman is accepting graduate students in her laboratory. Dr. Ashman is accepting undergraduate researchers, and does sponsor students in other laboratories.

Professional Interests - Publications - Contact Information - Lab Personnel

Professional Interests of Tia-Lynn Ashman

Clarkia tembloriensisWhy are some plants male or female whereas others are both? Why are some flowers showy and fragrant while others are plain and faintly scented? Why do some flowers live for months and others live for only a few hours? The research in my lab aims to address these, and other questions by studying the evolution of separate sexes and floral phenotype within the general constructs provided by life history and sex allocation theories, and by integrating the study of plant-animal interactions (e.g., pollination and herbivory), physiological and chemical ecology with quantitative genetics and evolutionary biology.

Currently, a major focus of the lab is addressing a question that has intrigued evolutionary biologists since Darwin, that is, how separate sexes (dioecy) evolved from combined sexed ancestors (hermaphrodites). We still don't have a complete picture of how this transition occurs, but an intensively modeled theory predicts that populations with females and hermaphrodites are an intermediate step to dioecy. We aim to go beyond description of reproductive variation to comprehensively evaluate the roles of adaptation and constraint in the evolution of separate sexes and sexual dimorphism using wild strawberry (Fragaria virginiana) and a quantitative genetic model as a framework for this research.

Strawberry fruits What conditions generate selection for males in gynodioecious populations? One main objective is to determine the conditions necessary for hermaphrodites of gynodioecious species to be selected to become more male, i.e. the conditions that facilitate the "second step" in the evolution of dioecy. Our work and that of others suggest that maleness may be favored when females are frequent and soil resources are scarce. In a collaboration with Dr. Mary Ashley at UIC, we are testing the hypothesis that certain ecological contexts intensify selection for maleness of hermaphrodites by manipulating female frequency and resource availability in arrays of plants and then quantifying phenotypic selection on pollen production, and other male traits, directly with the aid of microsatellite DNA markers to determine male fitness. This work will be the first to provide not only an understanding of the selective dynamics of the gynodioecy-dioecy transition, but also the first to directly address theory-based predictions regarding the environmental causes of selection for maleness.

Pollen grains germinating on the styles of Sidalcea oregana What are the constraints on the evolution of males from hermaphrodites? A second goal of our research has been to assess the universality of genetic constraint imposed on the independent evolution of sexual phenotype and determine if constraints differ under different selective regimes (i.e., female frequencies), as well as to rigorously test the genetic assumptions of sex allocation theory under field conditions. We have revealed broad-sense heritability for male and female traits of hermaphrodites, as well as, a negative genetic correlation between pollen production and fruit setting ability, and thus have verified basic assumptions of sex allocation theory. We are now in the process of determining the degree of narrow sense genetic variation and genetic correlation between sexual traits shared by the sex morphs (e.g., ovule number and fruit set) in populations of wild strawberry that differ in their female frequency, and thus represent different stages along the gynodioecy-dioecy continuum.

The Weevil What role do enemies play in the evolution of males from hermaphrodites? Recently, our research has turned to a little explored aspect of the environmental context for the evolution of dioecy, that is, the enemy dimension of the environment. Herbivory in dimorphic species can be profoundly male-biased, and we are exploring whether herbivores hold the key to why traditional explanations for breeding system variation sometimes fall short. We are using the wild strawberry and it's flower bud-clipping herbivore (Anthonomous signatus) as a model system to explore several novel hypotheses as to how male-biased herbivory may impede the transition from gynodioecy to dioecy. Ultimately, we aim to expand our understanding of the environmental context for the evolution of dioecy beyond abiotic attributes and mutualists to include enemies.

Ashman lab at work How and when does sexual dimorphism in attractive traits evolve? While it is well established that male plants are more attractive (i.e., have larger flowers and more of them) than female plants, it is not clear how this sexual dimorphism comes about. Traditionally, pollinator-mediated selection that acts differently through male and female fitness has been invoked to explain sexual dimorphism. To begin to understand the role that pollinator behavior plays in the evolution of attractive traits (petal and stamen size) in F. virginiana my lab has conducted a set of interrelated experiments in which we manipulated several aspects of flower phenotype, sex ratio, and pollinator fauna and then measured plant fitness response. Our results indicate that 1) a whole suite of characters contribute to the greater attractiveness (to pollinators) of hermaphrodite flowers relative to female flowers, 2) only certain conditions generate male-biased selection, and thus could lead to selection-driven male-biased petal size dimorphism, 3) flexible pollinator foraging may be an important mechanism by which sex ratio influences selection on attractive traits, 4) variation in sex ratio could limit the evolution of sexual dimorphism, and/or could maintain genetic variation in attractive traits. In addition, results from quantitative genetic experiments suggest that the sex morphs may not be equally capable of responding to selection. We are currently extending this line of inquiry to whole plant traits and to directly measure male fitness to get the first glimpse at how sexual dimorphism and gender coevolve.

A common theme of the research in my lab is to determine how the floral phenotype is shaped by selection through pollinators, herbivores and/or the abiotic environment. We often explore this in the context of sexual dimorphism because the sex morphs provide an elegant natural comparison. However, we are also interested in evolution of floral variation in general, and in terms of less well-studied characters, such as floral fragrance and longevity.

Artificial flowers Why are some flowers not very fragrant? Recently our lab has begun to explore how herbivores and pollinators respond to variation in floral odor in a collaboration with Dr. Robert Raguso at USC. We are determining the role of floral and pollen scent in bringing about sex differences in attractiveness of strawberry flowers to herbivores (clipper weevils) and pollinators by offering fragrance enhanced artificial flowers, natural buds and flowers to insects and quantifying their responses. We aim to determine if strawberry floral fragrance is under opposing selection pressures through pollinators and herbivores, and if this is why they are so weakly scented.

How long should flowers live? An on-going interest in the lab is the evolution of flower longevity. We have, in collaboration with Dr. Daniel Schoen at McGill University, studied the adaptive significance of flower life time. This work has shown that the optimal flower longevity of a species or population reflects the balance between the relative cost of flower construction and maintenance, and the accrual rates of pollen deposition and removal.


Publication Archive
50 Citations
45 Abstracts
42 PDFs

Recent Publications of Tia-Lynn Ashman

Steets, J.A., D.E. Wolf, J.R. Auld, and T.-L. Ashman (2007) The role of natural enemies in the expression and evolution of mixed mating in hermaphrodite plants and animals. Evolution 61:2043-2055 (PDF Reprint: 148 kb)

Case, A.L., and T.-L. Ashman (2007) An experimental test of the effects of resource and sex ratio on maternal fitness and phenotypic selection in gynodioecious Fragaria virginiana. Evolution 61:1900-1911 (PDF Reprint: 178 kb)

Steets, J.A., T.M. Knight, and T.-L. Ashman (2007) The interactive effects of herbivory and mixed mating for the population dynamics of Impatiens capensis. Am. Nat. 170:113-127 (PDF Reprint: 401 kb)

Ashman, T.-L., and L. Penet (2007) Direct and indirect effects of a sex-biased antagonist on male and female fertility: consequences for reproductive trait evolution in a gender dimorphic plant. Am. Nat. 169:595-608 (PDF Reprint: 382 kb)

Majetic, C.J., R.A. Raguso, S.J. Tonsor, and T.-L. Ashman (2007) Flower color-flower scent associations in polymorphic Hesperis matronalis (Brassicaceae). Phytochemistry 68:865-874 (PDF Reprint: 219 kb)

Knight, T.M., J.A. Steets, and T.-L. Ashman (2006) A quantitative synthesis of pollen supplementation experiments highlights the contribution of resource reallocation to estimates of pollen limitation. Am. J. Bot. 93:271-277 (PDF Reprint: 165 kb)

Steets, J.A., R. Salla, and T.-L. Ashman (2006) Herbivory and competition interact to affect reproductive traits and mating system expression in Impatiens capensis. Am. Nat. 167:591-600 (PDF Reprint: 437 kb)

Steets, J.A., J.L. Hamrick, and T.-L. Ashman (2006) Consequences of vegetative herbivory for the maintenance of intermediate outcrossing in an annual plant. Ecology 87:2717-2727 (PDF Reprint: 156 kb)

Ashman, T.-L. (2006) The evolution of separate sexes: A focus on the ecological context. Pp 419-465 in The Ecology and Evolution of Flowers, Harder, L.D., and S.C.H. Barrett, Ed. Oxford University Press, Oxford (PDF Reprint: 191 kb)

Delph, L.F., and T.-L. Ashman (2006) Trait selection in flowering plants: how does sexual selection contribute? Integr. Comp. Biol. 46:465-472 (PDF Reprint: 108 kb)

Ashman, T.-L., and C.J. Majetic (2006) Genetic constraints on floral evolution: A review and evaluation of patterns. Heredity 96:343-352 (PDF Reprint: 173 kb)

Vamosi, J.C., T.M. Knight, J.A. Steets, S.J. Mazer, M. Burd, and T.-L. Ashman (2006) Pollination decays in biodiversity hotspots. Proc. Natl. Acad. Sci., USA 103:956-961 (PDF Reprint: 545 kb)

Ashman, T.-L. (2005) The limits on sexual dimorphism in vegetative traits in a gynodioecious plant. Am. Nat. 166:S5-16 (PDF Reprint: 463 kb)

Knight, T., J.A. Steets, J.C. Vamosi, S.J. Mazer, M. Burd, D.R. Campbell, M. Dudash, M.O. Johnston, R.J. Mitchell, and T.-L. Ashman (2005) Pollen limitation of plant reproduction: Pattern and Process. Annu. Rev. Ecol. Evol. S. 36:467-497 (PDF Reprint: 220 kb)

Ashman, T.-L., D.H. Cole, M. Bradburn, B. Blaney, and R.A. Raguso (2005) Scent of a male: the role of floral volatiles in pollination of a gender dimorphic plant. Ecology 86:2099-2105 (PDF Reprint: 154 kb)


How to Contact Tia-Lynn Ashman

US Mail
University of Pittsburgh
Department of Biological Sciences
204 Clapp Hall
4249 Fifth Avenue
Pittsburgh, PA 15260
  Phone, FAX, Internet
Office : (412) 624-0984
Lab : (412) 624-0985
FAX : (412) 624-4759
Email : tia1+@pitt.edu
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