“Willed Women”: Studying Medieval Literature at OSU

An image of the second nun from Chaucer’s Canterbury Tales

When asked to trace her love of literature to its origins, Emily McLemore returns to her babyhood. “My dad started reading to me from the day I was born, so my love of reading started early,” she says. Last month, Emily defended her Master of Arts thesis, “Willed Women: Female Bodies & Subversive Being in the Knight’s and Second Nun’s Tales.”

Her path to studying medieval literature began as an undergraduate at Western State Colorado University. Before attending WSCU, she worked a series of jobs but always knew that she wanted to return to college and become a teacher. Emily studied English, with an added emphasis in Secondary Education, but when she began student teaching in an eighth grade classroom, she quickly realized it wasn’t for her. She had read Beowulf in one of her undergraduate courses, and that experience helped her recall what she loves about literature and textual analysis: learning to illuminate the complexities of a narrative to understand its meanings and cultural connections.

Emily McLemore

She applied to one graduate school program—the MA in Literature and Culture at Oregon State—and was admitted with a position as a Graduate Teaching Associate. Once at Oregon State, she met with Professor Tara Williams, who recommended that she read the Second Nun’s Tale, one of the lesser-known Canterbury Tales by Geoffrey Chaucer. Emily began to consider how women, gender, and sexuality studies might be a lens through which to read this tale. Along with another Canterbury Tale, the Knight’s Tale, she formed an argument around how the women in these texts employ their bodies and their sexuality to confront and subvert patriarchal power structures. Her thesis tackles these two tales and their “willful women,” a subject that she presented on last month at the International Congress on Medieval Studies. Emily will continue to study these works and other medieval texts this fall as she begins a PhD in English at the University of Notre Dame.

The Ellesmere Chaucer, a 15th century manuscript of the Canterbury Tales.

To learn more about Emily’s research and her path to graduate school, tune in to hear our conversation on Sunday, June 11th at 7:00 pm on 88.7 FM KBVR Corvallis or listen live online.

Do you trust others, as much as they trust you?

My mother told me never to judge a book by its cover, but our brains do this tens if not hundreds of times a day. Research has shown that seeing a face for just 1/10 second allows enough time for someone to make judgments of a person’s attractiveness, competence, aggressiveness, and trustworthiness. While it is impressive our brains can come to a decision about a face so quickly, how accurate are those assessments? For better or worse, a person’s facial characteristics can predict court decisions, as well as outcomes of elections. Many studies focus on how the interpreter makes these decisions, but what happens to the people who are instantly considered untrustworthy when all you see is a face? Whether we care to acknowledge it, these first-impressions inevitably lead to different life-outcomes, especially if you are judged as having an untrustworthy face.

What kind of facial features can be considered trustworthy or untrustworthy? Here are some examples on a spectrum.

Our guest this evening is Zoe Alley, a 1st year PhD student in the newly formed Psychological Sciences program within the College of Liberal Arts, and she will be tackling these tough questions of how we perceive and understand trust. She is specifically exploring how the first impression of someone’s face can be a predictor, or possibly a driver, of their future life-outcomes. The Golden Rule says to treat others the way you want to be treated; but what happens when everyone around you is unpleasant or treats you with suspicion? You’re more likely to reciprocate those feelings, developing fewer formative relationships early in life, eventually snowballing into awkward social behaviors intensifying later in life so that finding a job or keeping friends are hopeless endeavors. Was this sequence of events caused by the person’s actions toward others, or was it the constant distrust from others that caused these behaviors leading to a negative outcome?

This is a classic chicken or the egg dilemma that we will explore, but first we have to understand how we got here. The Oregon Youth Study began in 1982 with evaluations of participants starting at age 10, and continuing with annual assessments until all 183 males from predominantly lower income neighborhoods reached 35 years old. This study generated a prodigious amount of data that scientists continue to use. One finding was the participants’ real-life behavior explained relatively small but measurable amount of how trustworthy those outside the study perceived them to be once other factors  were controlled (i.e. smiling). This shows a disconnect from how we judge someone, compared to how that person actually behaves. This again begs the question: what happens to those unfortunate souls who are constantly judged negatively and is there anything we can do mitigate this unfortunate pattern?

Here is Zoe Alley who is a 1st year PhD student in the Psychological Sciences program at OSU

Zoe grew up as a native Oregonian and while her childhood passion started with art and expression, it has always focused on how she can help her community. Even though the Oregon Youth Study was focused in the Willamette Valley, understanding these social constructs can help children and adults everywhere. Through this research Zoe hopes to understand how this phenomenon of ‘facial trustworthiness’ works, especially in adolescents, so that we can identify mechanisms to break this vicious cycle and give everyone an equal chance at success. Be sure to tune in for what is sure to be a candid discussion on Sunday June 4th at 7PM on KBVR Corvallis 88.7FM or by listening live.

 

Heliconia: plants with personality

Orange-hatted Dusty Gannon’ (my hummingbird name) visiting Heliconia tortuosa

In the Department of Botany and Plant Pathology, first year graduate student Dusty Gannon is studying how Heliconia tortuosa, a tropical plant with long, tubular flowers and vividly-colored bracts (modified leaves that house the flowers), maintains its unique relationship with pollinating hummingbirds. Although hummingbirds universally love nectar, they have diverged into a few distinct functional groups that are characterized by behavior: traplining hummingbirds repeatedly and circuitously visit flowers, often traveling long distances, while territorial hummingbirds are aggressively possessive of flowers in a home range. It turns out that Heliconia tortuosa is picky about which of these groups contributes to its pollination, and preferentially accepts pollen from traplining hummingbirds, specifically those featuring a long, curved bill. Presumably, their bill shape facilitates maximal nectar extraction which is used as a cue by the plant to become receptive to pollen.  Many hummingbirds visit the Heliconia tortuosa flower, but few induce pollination because of the straight shape of their bill. The shape and size of the Heliconia tortuosa flower in relation to the shape and size of the beak of the pollinator hummingbird constitutes the emergence of a complex plant behavior.

Heliconia wagneriana

Heliconia wagneriana

 

 

 

 

 

 

 

 

 

Dusty’s research is focused on trying to understand how Heliconia tortuosa evolved the capacity to recognize and preferentially invest in pollination by certain pollinator hummingbirds. His work consists of testing for ‘pollinator recognition’ of pollinators across a select subset of species across the Heliconia genus, comprised of 200-250 species, and subsequently using molecular techniques to infer the presence or absence of pollinator recognition across
 the family. Among these several hundred different species of Heliconia, the flowers are morphologically distinct and vary in size from short to long,  straight to curved (even up to a 90-degree angle!). Dusty’s objective is to determine if pollinator recognition is a common trait among morphologically distinct Heliconia species, and uncover the evolutionary significance of this cryptic specialization. While conducting fieldwork at Las Cruces Biological Station in Costa Rica, which featured a garden full of Heliconia, Dusty collected over 1,000 styles (the female reproductive organ in flowering plants) to assay pollen-tube growth rates across various treatments by epi-fluorescence microscopy back at OSU.

Tropical montane forest

Unraveling the tangled evolutionary biology of plants and pollinators is critical for understanding how the loss of certain pollinators might impact plant pollination. If a flower is visited by a variety of different pollinators, the loss of one pollinator might not seem like a big deal. However, if only a small number of the total number of pollinators visiting the flower are capable of inducing pollination, the loss of a true pollinator might be devastating for a plant’s ability to reproduce.

A sample of the morphological diversity in Heliconia flowers

As an undergrad at Colorado State University, Dusty studied Ecosystem Science, which consisted of learning about how nutrients and energy flow through an ecosystem. Dusty cites his high school AP Biology teacher as having a major influence on his desire to study science in college. During the first week of his freshman year, Dusty applied to work in a lab doing DNA barcoding; over the span of 4 years, he conducted over 10,000 PCR reactions! Following completion of his undergrad, Dusty planned to climb mountains in South America for a year, but unexpected circumstances expedited his enrollment in graduate school at OSU to pursue research related to pollinator recognition. Following completion of graduate school, Dusty would like to continue in academia as a professor, and possibly open a bread shop featuring a wood-fired oven, equipped with statistical models to ensure a perfect loaf of bread.

Join us on Sunday May 21st at 7PM on KBVR Corvallis 88.7FM or stream live to hear more about Dusty’s pollinator recognition research and journey through graduate school.

Motor proteins—and people—can change directionality

It took three years of adventures after college—including stints as a ski instructor, barista and a commercial chemist—before Andrew Popchock knew that he wanted to return to the lab to pursue a PhD at OSU’s Department of Biochemistry and Biophysics.

Two microtubules slide across each other by the walking of motor proteins sandwiched between them

Andrew’s research takes place at Dr. Weihong Qiu’s Single-Molecule Biophysics Laboratory and focuses on kinesin-14s—motor proteins found in eukaryotic cells. These motor proteins in cells travel along microtubules to create and maintain the mitotic spindle, which are macromolecular structures that are responsible for chromosome segregation during cell division.

By using an imaging technique called TIRF microscopy, a team of researchers from Dr. Qiu’s lab discovered that a kinesin-14 found in fungus cells called KlpA can change direction along its cytoskeleton tracks. KlpA is the first motor protein of its kind that researchers have discovered that demonstrates this type of bidirectional movement. The results of their study were recently published in Nature Communications.

Total Internal Reflection Fluorscence (TIRF) microscopy image of two microtubules sliding across each other

The motor protein that Andrew studies could be important in helping researchers understand cancer growth. This could have implications for drug treatment therapy, potentially guiding the creation of motor protein-based molecular devices for more controlled drug delivery in cancer treatments.

 

Andrew on the Oregon Coast

Growing up, Andrew was interested in physics and biology, but it wasn’t until he worked in a lab under the direction of a graduate student at Washington State University that he began to consider graduate studies. While working as a chemist in Idaho, he realized that he quickly reached the limit of his creative capacity and that returning to a laboratory as a graduate student at OSU would help him continue to develop his skills as a researcher.

To learn more about Andrew’s research and his path to graduate school, tune in to hear our conversation on Sunday, May 14th at 7:00 pm on 88.7 FM KBVR Corvallis or listen live online.

Bone marrow transplants save lives, but can it keep our bones strong?

What doesn’t kill you makes you stronger. This phrase is often helpful when fighting adversity, but it does not hold true for patients suffering from diseases such as leukemia, tuberculosis, and certain forms of anemia. Current medical science allows us to save lives, but their quality of life is curtailed because bones are typically weaker and prone to breaking as a result of cancer treatments. Patients may have endured countless surgeries, drug rehabilitation, and physical therapy only to have their level of physical activity severely limited because of the complications posed from fragile bones.

Goldner’s trichrome staining, in which mineralized bone matrix, erythrocytes, and cytoplasm were stained green, orange, and red, respectively. Credit: Burr, David B., and Matthew R. Allen, eds. Basic and applied bone biology. Academic Press, 2013.

At the center of this problem is bone marrow, and working to find a solution is Richard Deyhle, a Masters student studying Radiation Health Physics, believes we may have found a way to treat these cancers while also increasing our bone strength to previous levels of functionality. This work is in the proof-of-concept phase so it’s still early in the framework of medical application to the public but there is little doubt this can provide miraculous benefits to cancer patients providing them a higher quality of life.

Richard working on generating a 3D visualization of Micro-Computed Tomography data.

 

First it’s important to understand that even though bone marrow only accounts for ~4% of our body mass, it’s also the production source of red blood cells (carrying oxygen throughout our body), blood platelets (helping to clot blood to prevent blood loss), and white blood cells (major players in our immune system keeping us healthy). Cancer treatments focus on treating and restoring the healthy function of bone marrow so we can live. Kind of important stuff! But the health of the bone marrow does not always correspond to strong bones. This is where Richard, working under Urszula Iwaniec & Russell Turner in the Skeletal Biology Lab at OSU, brings their expertise to find new ways to treat malfunctioning bone marrow.

Micro-Computed Tomography image of the radius bone from a rat from Space Shuttle Mission, STS-41.

Bone marrow is made of many subcomponents, and standard medical practice is to replace a patient’s bone marrow (containing all subcomponents) with bone marrow from a compatible donor. Depending on the extent of transplant, there are somewhere in the neighborhood of 5,000,000 cells that are replaced representing the mosaic of cells that make up bone marrow. Richard is using a more targeted approach of purifying bone marrow and isolating a subcomponent, called Hematopoietic stem cells, so a transplant will only need a few thousand of these special cells to perform the same function as the much larger transplant. Using mice models his lab has found similar results as other researchers showing the use of pure Hematopoietic stem cells, instead of bulk bone marrow material, has similar effects on bone marrow functionality. Through the use of Green Fluorescent Protein (as a bookmark in the newly injected cells allowing researchers to trace where cells move through the body), the Skeletal Biology Lab hopes to better understand the mechanism of bone strength resilience to a healthy functioning bone marrow. Like any good scientific study, much more work needs to be done to examine these results and verify effect sizes, but the road ahead looks promising.

Richard’s childhood home was nestled away from large cities that allowed him to stare at the sky and see the Milky Way in all its beauty. Even at a young age he wondered about space, wondered how far humans can go, and wondered how he can help keep future explorers safe as we explore distant worlds. These youthful curiosities of space eventually lead to his research passion of understanding how radiation affects the human body. If all his plans work out he hopes to transition into a PhD program where he can focus more closely on making sure our fragile human bodies can explore worlds beyond ours.

If you’re interested in new medical advancements that can be used to treat cancer or astronauts, you cannot miss this episode! Be sure to tune in Sunday May 7th at 7PM on KBVR Corvallis 88.7FM or by listening live.

Keeping Oregon Forests Green: What Swiss Needle Cast Disease is Teaching Us About Forestry

I’ll never forget driving through the steep and windy I5 corridor of the Klamath Mountains when I moved to Oregon. Wet roads bordered by thick fog with protruding trees that were lusciously green. Very, very green. This concept of ‘Keeping Oregon Green’ started as a fire prevention act, and Oregon’s color is a quality that visitors and residents adore. Unfortunately there is sleeping giant that is gaining momentum, slowly turning Oregon’s forests from green to yellow with an eventual needle fall of the iconic state tree. This color change is from a microscopic fungus that all Douglas-fir trees have around the world, but for some reason it’s only harming the trees along the Oregon coast range. Our guest, a 4th year PhD student Patrick Bennett, is peeling away the layers of complexity to reveal why Oregon’s green forests are dwindling.

Aerial view of Douglas-fir stand with Swiss needle cast near Tillamook, Oregon. Chlorotic (yellow) foliage is a major symptom of the disease.

Douglas-fir needles with pseudothecia (fruiting bodies) of the fungus (Phaeocryptopus gaeumannii) emerging from the stomata.

It is estimated that Swiss Needle Cast disease is affecting nearly 1,000,000 acres in Oregon and Washington alone leading to economic losses estimated at $128 million per year. The fungus covers the stomata, openings in the needles, used to exchange air and water essential for plant metabolism. As more of these stomata become clogged the tree cannot make enough glucose so the needle dies, turns yellow, and eventually the needle falls off entirely. Douglas-fir trees typically keep needles for five years, but in heavily affected areas the needles last one year before falling off leaving the tree extremely thin and frail. Even though the fungus does not directly cause death, it leaves our iconic state tree highly susceptible to drought, beetles, nutrient limitations, and wildfires.

This disease was first discovered in Switzerland, hence the name Swiss Needle Cast, in the 1920’s. At that time it was only negatively affecting Douglas-fir trees planted outside their native habitat. But since the 1980’s the natively planted Douglas-fir trees, within a narrow band parallel to the coast range, are showing annual growth decreases by as much as 50%. Recently there have been advancements in molecular biology and computing power that allow researchers to identify the genetic heritage of pathogens. Using these tools scientists can focus on population genetics to figure out why there is such a discrete area affected along the Oregon coast range. Some evidence points to  warming winters and fungal-subspecies expansion as reasons for the spread of this fungal disease. But Patrick has indications to suggest it’s death by a thousand cuts and begs the question of whether the future of forestry is in danger.

Growing up in southern California Patrick wasn’t exposed to the forests he studies today. It wasn’t until he attended Humboldt State University where he got his first exposure to towering canopies and ecology. His first research experience was in the Lassen Volcanic National Park in California where his advisor, Dr. Patricia Siering, pushed him to develop his own scientific study. Needless to say he was hooked on science and after taking a mycology class he also knew he was jazzed on studying mushrooms so he continued his passions that lead him to Oregon State University.

Dr. Patricia Siering (Humboldt State University – Biology Department) collecting boiling hot sulfuric acid from Boiling Springs Lake in Lassen Volcanic National Park in Northern California with the help of undergraduates and graduate students.

Patrick Bennett is a 4th year PhD student in Dr. Jeff Stone’s lab in the department of Botany and Plant Pathology housed in the College of Agricultural Sciences where he is investigating how population genetics can be used to better understand the factors contributing to the recent emergence of Swiss Needle Cast as a damaging forest pathogen in the native range of Douglas-fir. Be sure to tune in Sunday April 30th at 7PM on KBVR Corvallis 88.7FM or by listening live.

Elucidating protein structure with crystals

Kelsey in the lab pipetting one of her many buffers!

Proteins are the workhorse molecules of the cell, contributing to diverse processes such as eyesight, food breakdown, and disabling of pathogens. Although cells cannot function without helper proteins, they’re so small that it’s impossible to view them without the aid of special tools. Proteins are encoded by RNA, and RNA is encoded by DNA; when DNA is mutated, the downstream structure of the protein can be impacted. When proteins become dysfunctional as part of disease, understanding how and why they behave differently can lead to the development of a therapy. In Andy Karplus’ lab in the Department of Biochemistry & Biophysics, PhD candidate Kelsey Kean uses a technique known as protein x-ray crystallography to study the relationship between protein structure and function.

Protein crystals. On the left, each blade making up this cluster is an individual crystal that needs to be separated before we can use them.

Protein diffraction. An individual crystal is placed in front of an x-ray beam and we collect the diffraction resulting from the x-ray hitting each atom in the protein crystal . Using the position and darkness of each spot (along with some other information), we can figure out where each atom in the crystal was originally positioned.

An electron density map. After collecting and processing our diffraction images, we get an electron density map (blue)- this shows us where all the electrons for each atom in the protein are- and this guides us in building in the atomic coordinates (yellow) for each part of the protein. It’s like a puzzle!

Crystallization of protein involves many steps, each of which presents its own unique challenges. A very pure protein sample is required to form an ordered crystal lattice, and hundreds of different buffer solutions are tested to find the ideal crystallization conditions. Sometimes crystals can take weeks, months, or a year to grow: it all depends on the protein. Once a crystal is obtained, Kelsey ships it to the synchrotron at Lawrence Berkeley National Laboratory, which provides a source of ultra powerful x-ray light beams. Exposure of the protein crystal to x-ray light results in a diffraction pattern, which is caused by the x-ray light diffracting off of all the atoms in the crystal. A map of electron density is generated from the diffraction pattern, and then the electron density map is used to determine where the atoms are located in the protein, like a complex puzzle. X-ray protein crystallography is really amazing because it allows you to visualize proteins at the atomic level!

In addition to her lab work, Kelsey is extensively involved in teaching and STEM outreach. For the past 3 summers, she has organized a week-long summer biochemistry camp through STEM Academy, with the help of a group of biochemistry graduate students. Kelsey has also been involved in Discovering the Scientist Within, a program providing 150 middle school girls with the opportunity to perform science experiments, including isolation of strawberry DNA and working with mutant zebrafish.

Kelsey completed her undergraduate degree in biochemistry with a minor in math at the University of Tulsa, where she was also a Division I athlete in rowing. She attributes her work ethic and time management skills to her involvement in Division I athletics, which required a significant commitment of time and focus outside of lab and coursework. During one summer when she wasn’t busy with competitive rowing, she performed experiments related to protein crystallography at the Hauptman-Woodward Medical Research Institute associated with the University at Buffalo.

Kelsey knew she wanted to pursue science from an early age. She grew up surrounded by scientists: her mom is a biochemist and her dad is a software engineer! She recalls playing with Nalgene squirt bottles as a kid, and participated in the Science Olympiad in middle school, where she engineered a Rube Goldberg machine. She cites early exposure to science from her family as one reason why she feels strongly about STEM outreach to students who might not otherwise receive encouragement or support. In the future, Kelsey would like to teach at a primarily undergraduate institution.

Please join us this Sunday, April 23rd on KBVR Corvallis 88.7FM at 7 pm PST  to hear much more about x-ray protein crystallography, STEM outreach, and to hear an awesome song of Kelsey’s choosing! You can also stream this episode live at www.kbvr.com/listen.

Beetle-Seq: Inferring the Phylogeny of Clivinini

We humans are far outnumbered by organisms that are much smaller and “less complex” than ourselves. The cartoon above depicts representatives of major groups of organisms, and each organism is drawn such that its size reflects the number of species contained within its group. The bird, the fish, and the trees look as expected, but you may notice the enormous beetle. No, beetles are not generally larger than trees or elephants, but there are more species of beetles than any other group of organisms. Beetles are a wonderful representative of the biodiversity of the earth because they can be found in almost every terrestrial and non-marine aquatic environment!

Examples of carabid beetles of the tribe Clivinini (top row; photos with ‘HG’ – Henri Goulet, otherwise – David Maddison). Male genitalia of a clivinine species, Ardistomis obliquata, with possible ‘copulatory weapons’ (right) and several examples of clivinine female genitalia (bottom row) modified from Zookeys 2012;(210):19-67 shared under CC BY 3.0.

Our guest this week, Antonio Gomez from the Department of Integrative Biology, studies a group of beetles called clivinines (pronounced kliv-i-nīnz) which has 1,200 species, and potentially more that have yet to be discovered. Antonio is also particularly interested in the morphological diversity and evolution of clivinine beetle sperm. Antonio wants to know: What is the evolutionary history of clivinine beetles? What is the pattern of morphological diversity of sperm in clivinine beetles, and how are sperm traits evolving? The objective is to collect beetles, study their form, sequence their DNA, and understand their diversification.

Several examples of sperm conjugates (cases where two or more sperm are physically joined and travel together) in carabid beetles. Conjugation is considered rare, but in carabid beetles, it’s the rule and not the exception to it. In many carabids, sperm leave the testis but do not individualize. Instead, they remain together and swim as a team.

This is no small task, but Antonio is well equipped with microscopes to dissect and describe beetle anatomy, a brain geared to pattern recognition, and some fresh tools for genome sequencing. All of this is used to build an evolutionary tree for beetles. This is kind of like a family tree, but with species instead of siblings or cousins. Antonio and other students in the lab of David Maddison are adding knowledge to the vastness of the beetle unknown, bit by bit, antenna by antenna, gene by gene.

Antonio Gomez collecting beetles near a really bright light (a mercury vapor light trap) near Patagonia, Arizona.

Like many of our graduate students at Oregon State, a group of great mentors can make all the difference. Before working with Dr. Kelly Miller at University of New Mexico, he never knew beetle phylogenetics meant exploring exotic locations around the world to collect and potentially discover new species. As an undergraduate, Antonio even named a species of water beetle, Prionohydrus marc, after the undergraduate research program that go him started as a beetle systematist, the Minority Access to Research Careers (MARC) program. Pretty amazing. That was not his first or last research project with insects before he joined ranks at Oregon State, he also was participated in a Research Experience for Undergraduate program at the California Academy of Sciences and completed a Master’s at University of Arizona. Now he has ample experience working with beetles and is maybe a little overwhelmed but still excited by the unknown beetle tree of life. Next on his list of questions: did the ancestor of all clivinines likely have sperm conjugation?

You’ll have to tune in on Sunday April, 16 at 7 pm to hear more about that evolutionary arms race!
Not in Corvallis? No sweat! Stream the show live.

Can’t get enough? Follow this link to learn about Stygoprous oregonensis, a blind subterranean diving beetle that had not been seen in 30 years. Recently, a team of researchers that included Antonio Gomez reported the discovery of more specimens, which allowed them to place Stygoporus in an evolutionary tree.

Just keep swimming or don’t! Curiously following Zebrafish

People often think of science as focusing on very specific questions or rigorous hypothesis testing. However, some of the most exciting advancements were the result of general curiosity of seemingly disparate ideas, and a sprinkle of creativity. For example, the beginnings of how electricity was discovered started by poking frog legs with different types of metals. The modern zero-calorie sugar (saccharin) was discovered by playing creative-chef with coal tar products in the 1870’s when the chemist accidentally tasted his chemical concoction.

Sarah Alto

Our guest this week is using young zebrafish to investigate how environmental factors affect their behavior, and whether behavioral changes can be attributed to specific brain activity. Why zebrafish you may ask? They are a model organisms or they tend to be well studied, relatively easy to breed and maintain in lab settings, and as vertebrates, they share some characteristics with humans. The more we know about zebrafish, the more clues we may have into our own neurobiology. Sarah Alto is exposing these model organisms to different levels of oxygen and carbon dioxide stress. She monitors their swimming with infrared cameras and examines their brain to get an idea of how they respond to stress physically and mentally. This is no easy task because the young zebrafish are only a few millimeters long!

Oxygen, nitrogen, and carbon dioxide gas is bubbled into the tank holding the larvae.
The entire set-up is enclosed in a light-tight box so the larval behavior is more connected to the environment changes and not human interaction.

Curious Sarah is asking: Are low oxygen or high carbon dioxide concentrations changing the swimming behavior of zebrafish? What happens in the brain of a zebrafish when it experiences environmental stress? What can we learn about how environmental factors shape the brain’s connections and influence behavior? Sarah has a long road ahead of her, one that is unpaved with many junctions, but she is performing the exploratory work that may inspire future investigations into the affects of stress on the brain.

The second part of Sarah’s research will be investigating the neural activity when the larvae are exposed to the same gas concentrations as studied in the behavioral experiments.
Image courtesy of Ahrens et al. (2013)

Prior to Sara’s interest in biology, she was always drawn to art as an escape and a method of expression. When choosing which colleges to attend, she didn’t want to choose between art and science. So she chose to pursue both! Sarah enrolled at UC Berkeley as double major including Molecular and Cellular Biology, as well as Practice of Art. The San Francisco art scene was highly accessible, and Berkeley is a top-flight university for the sciences. Needless to say she flourished in this environment and her love of science grew but her love of art continues to this day. Finishing her schooling she began working at UC San Francisco, a premier medical research university, investigating the role of stem cells in facial development to for possible medical treatments for facial reconstruction. She was involved in a variety of projects but her gut feeling led her to continue schooling at Oregon State.

Sarah is now a part of Dr. James Strother’s lab in the College of Science within the department of Integrative Biology focusing the behavioral neurobiology of zebrafish. Be sure to tune in Sunday April 9th at 7PM PST on 88.7FM or listen live.

Searching for viruses that make plants sick

Ripening sweet cherries in Mosier, Oregon. Photo credit: Lauri Lutes

When plants get sick, they can’t be treated or cured in the same way as people who receive medicine for an illness.  Plants require specialized care by scientists who are uniquely equipped to study and treat their diseases.  As a graduate student in the lab of Dr. Jay Pscheidt in the Department of Botany and Plant Pathology, Lauri Lutes is a plant doctor looking for viruses that infect sweet cherry trees in Oregon. She is able to identify an infected sweet cherry tree by looking at symptoms, including yellow rings or discolored mottling on the leaves, or fruit that is smaller than normal. To pinpoint the identity of the virus, further tests in the lab are performed.

Mottling and ringspot symptoms on sweet cherry, Prunus avium, in Umpqua Valley, Oregon. Photo Credit: Jay W. Pscheidt

Sweet cherries are one of Oregon’s top commodities, with 12,300 acres of sweet cherry production near the Dalles and Hood River, and 3,200 acres in the Willamette valley. There are a few viruses that the Oregon Department of Agriculture looks for each year, including Plum pox virus, a quarantine pathogen in the United States. However, if sweet cherry trees are infected with something other than the most common or most damaging viruses, they may never receive a diagnosis! Lauri works with the Oregon Sweet Cherry Commission to determine where diseased sweet cherry trees are located in Oregon. During her time at OSU, Lauri has discovered a virus infecting sweet cherry trees in the Dalles region that had never been reported in Oregon!

Lauri Lutes collecting leaf samples from sweet cherry trees in The Dalles, Oregon. Photo credit: Lauri Lutes

As an undergraduate student majoring in biology at Indiana University South Bend, Lauri discovered her passion for plant biology after taking a plant systematics course. Her undergraduate research consisted of studying fungal pathogens in a native waterleaf plant that grows in the forest floor of Indiana. Lauri attributes her positive experiences in undergraduate classes and research to female professors who provided encouragement and strong mentoring. After the birth of her daughter during her senior year of college, Lauri’s path toward attending grad school diverged, and she began working at a plant pathogen diagnostics company, Agdia, Inc. There, she used magnetic particles to purify viruses from plant material and co-developed a Technical Support Department. Curiosity driven, she found that she still wanted a deeper foundation in plant pathology, which led her to pursue graduate work at OSU.

View of Mount Hood from sweet cherry orchard in Parkdale, Oregon. Photo credit: Lauri Lutes

In addition to her work with sweet cherry tree viruses, Lauri is enrolled in the Graduate Certificate in College and University Teaching (GCCUT) program, and is active in science communication, having recently been selected to attend ComSciCon-PNW (Communicating Science Conference) in Seattle. After grad school, Lauri is considering teaching at the university level and continuing her involvement in science communication. As the first person in her family to complete an advanced degree, she hopes to inspire and expose her daughter to educational opportunities she might not have had otherwise.

Please join us this Sunday, April 2nd on KBVR Corvallis 88.7FM at 7 pm PST, to hear much more about Lauri’s journey through grad school, and her research about sweet cherry tree viruses. 

You can also stream this episode live at www.kbvr.com/listen.

View from a sweet cherry orchard in the Hood River, Oregon. Photo credit: Lauri Lutes