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Theresa
M. Culley Assistant Professor Ph.D, The Ohio State University Plant Biology |
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Address: |
Telephone: (513) 556-9705 FAX: (513) 556-5299 Email: theresa.culley@uc.edu |
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| Office/Lab Location: 724 Rieveschl Hall [Note that we have moved from our old lab in room 816] | ||
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In my lab, we are interested in the evolution of plant breeding systems and the interplay between the reproductive biology of a species (its pollination biology, seed production, susceptibility to herbivory, etc.) and population genetics. I incorporate both ecological and genetic approaches in my research because they both yield valuable insights into evolutionary questions. My current research interests can be separated into the following:
The Evolution of Invasiveness in the Callery Pear (Pyrus calleryana)
The Callery Pear (Pyrus calleryana) was originally introduced
into the United States
from China
in the early 1900's as a rootstock species and as a source for fireblight
resistance. It has quickly become one of the
most popular ornamental tree species planted in urban areas. Known as the
'Bradford', 'Aristocrat', 'Cleveland Select', etc. (see list), these cultivars are highly
desired for their springtime display of white showy flowers, vibrant fall leaf
color, and tolerance of excessive drought and pollution. Within the last
decade however, wild Pyrus calleryana have begun appearing and
multiplying in natural areas, especially disturbed sites along railroads, roads,
and along park boundaries. Furthermore, many cultivated Callery Pears in
urban yards have also begun producing fruits even though each cultivar is
self-incompatible. Many of these fruits are dispersed by introduced birds
such as starlings. In our lab, we are studying why Pyrus calleryana
is suddenly beginning to spread and becoming invasive. Based on a
combination of ecological and genetic studies, it now appears that the recent
expansion of Callery pear cultivars in some localities is due to intraspecific
hybridization between the widespread 'Bradford' cultivar and other newer
cultivars. This has been verified by hand-pollinations conducted in the
greenhouse between different cultivars and also through genetic analyses with
microsatellite markers specific for each cultivar. We are continuing to
study this intriguing species to understand the factors that contribute to the
evolution of invasiveness in an introduced species as well as to develop
practical suggestions for the prevention of its continuing spread within the
United States.
Interested in Invasive Plants? Check out the resources at
the Ohio Invasive Plants Council (OIPC) webpage.
This is a great organization for gathering information,
making contacts, and learning what you can do to reduce the impact of invasive
plants in our environment.
The Evolution and
Expression of Cleistogamy in Violets (Viola)

Many
Viola species have mixed mating systems because they produce both open,
chasmogamous (CH) flowers and closed, cleistogamous (CL) flowers on the same
individual. CH flowers are often assumed to be outcross-pollinated while CL flowers
are automatically self-pollinated. One purpose of my research in
Viola is to determine why these two very different types of flowers are
produced, using two violet species found in the northeastern United States,
Viola pubescens and V. canadensis. Contrary to the assumption that
showy CH flowers are primarily outcross-pollinated, CH flowers exhibit delayed
selfing and are capable of variable levels of selfing (s = 0.07-0.60). In
addition, a low level of inbreeding depression (0.10) expressed in CH flowers is
consistent with a selfing species. CH flowers also appear to be responsible for
a larger portion of seed production than CL flowers. In general, it appears that
the dual system of chasmogamy and cleistogamy in Viola is a means of
adapting to unpredictable pollinators in the early spring (through outcrossing
of CH flowers when pollinators are present and delayed selfing in CH flowers
when pollinators are absent) and to a lack of pollinators during the rest of the
season (through CL flowers). In addition, energetic costs may be important
because costly CH flowers are produced in the early spring when light
availability is highest, while reduced CL flowers appear in the shaded
understory after the forest canopy forms. Read More...Genetic and Ecological Effects of Habitat Fragmentation
Fragmentation of natural areas may result in a decrease in population-level
genetic variation as well increased genetic differentiation. This topic is of
particular importance in the temperate deciduous forest in North America because
of widespread deforestation that has occurred over the past two centuries. Ohio
is one region that has been greatly affected as the amount of forested land in
the state declined from 95% in the early 1700's to 10% by 1910. Today,
approximately 31% of land in Ohio is forested. This pattern has created many
agricultural woodlots, in which plant populations are forced to persist. I have collaborated with
Thomas Grubb
Jr. on a study of Viola pubescens examining the genetic effects of
habitat fragmentation. Evidence now suggests that the species has indeed been
negatively affected by fragmentation; genetic variation was lowest in
populations found in the smallest woodlots, while those in larger woodlots were
genetically variable. Genetic differentiation among populations was also
detected (Fst = 0.27), and is consistent with the CH/CL breeding system.
Selfing through CH and CL flowers may reduce genetic variation and promote
differentiation, but occasional outcrossing through CH flowers may prevent
populations from becoming completely differentiated from one another. I am
currently conducting a similar study in southwestern Ohio using urban
populations of V. pubescens to better understand how habitat
fragmentation induced by urbanization might affect this species.
Population Genetics and Plant Mating Systems

I am also interested in the genetic consequences of plant mating
systems, as measured with different molecular techniques. Together with
Andrea Wolfe at The Ohio
State University, we quantified the genetic structure in six populations of
Viola pubescens using isozymes and inter-simple sequence repeats (ISSRs).
Both markers showed considerable genetic variation with moderate population
substructuring. This is consistent with the mating system of the species, in
which selfing through CL (and CH) flowers contributes to population
differentiation, and outcrossing through CH flowers increases variation and gene
flow among populations. I have recently developed microsatellite markers
for V. pubescens and am currently comparing the genetic results generated
by microsatellites, isozymes, and ISSR makers.
For protocols of all types used in my lab, see the
Protocol Page...
The Evolution of Dioecy in the Hawaiian
Genus Schiedea.
Breeding system evolution is also the subject of my research with Schiedea,
a genus that has undergone extensive radiation in the Hawaiian Islands and
contains a full range of breeding systems - including hermaphroditism,
gynodioecy (co-occurrence of females and hermaphrodites), and dioecy
(co-occurrence of females and males). I am currently working with Drs.
Stephen Weller,
Ann Sakai, and
Diane
Campbell on a quantitative genetics experiment in which we are conducting
artificial selection to study the genetic potential for sex allocation shifts to
male and female function in two gynodioecious species, Schiedea salicaria
and S. adamantis. Many traits
associated with increased male and female function have a heritable basis and
thus may contribute directly to the evolution of dioecy. In addition,
we also measured the quantitative genetics of ecophysiological traits using
plants from our initial crossing program for both species. We found that some
ecophysiological traits are heritable, but only in certain sexes within
different species. This is of particular importance
because the heritability of ecophysiological traits have rarely been measured on
the scale of our study.
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